Nervous System Flashcards

1
Q

Huntington disease mode of inheritence

A

Autosomal dominant

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2
Q

Huntington disease is caused by an increase in _______ in the gne that codes for the huntingtin protein

A

CAG trinucleotide repeats

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3
Q

Expansion of the huntingtin protein’s polyglutamine region in huntington disease results in ________ which leads to pathological interaction with other proteins, including various transcription factors

A

Gain-of-function

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4
Q

in huntington disease, abnormal hintingtin causes increased histone ____ which silenes the genese necessary for neuronal survival

A

Deacetylation

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5
Q

Occlusion of the PICA results in _____ syndrome

A

Lateral medullary (Wallenberg)

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6
Q

PICA arises from what artery

A

Vertebral

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7
Q

What arteries course through the transverse foramina in the neck before entering the skull at the foramen magnum and therefore can be easily injured by cervical spinal trauma

A

Vertebral

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8
Q

Oclussion of which vessel is characterized by vertigo/nystagmus, ipsilateral cerebellar signs, loss of pain/temperature sensation in the opsilateral face and contralateral body, bulbar weakness and ipsilateral horner syndrome

A

Posterior inferior cerebellar artery

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9
Q

Blood pressure above ____ increases verebral vascular volume and blood flow, causing a corresponding increase in ICP

A

150 mmHg

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10
Q

Blood pressure below _____ causes cerebral hypoperfuion and potential ischemia

A

50 mmHg

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11
Q

A drop in PaCO2 whill have what effect on intercranial blood flow

A

Causes vasoconstriction –> decreases cerebral blood volume –> decreased ICP

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12
Q

Lowering ____ is one of the measures employed to reduce ICP in mechanically ventilated patients with cerebral edema

A

PaCO2

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13
Q

Carbon dioxide is a potent ____ of cerebral vasculature

A

Vasodilator

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14
Q

The anterior pituitary is derived from what embryonic tissue

A

Surface ectoderm

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15
Q

Bitemporal hemianopsia, amenorrhea, and elargement of the pituitary gland on brain imaging are suggestive of ___________

A

Prolactin secreting pituitary adenoma

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16
Q

Prolactinomas develop from ____ cells in the anterior pituitary (adenohypophysis)

A

Lactotroph

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17
Q

What occurs at 3 eks of embryogenesis resulting in 3 germ layers

A

Gastrulation

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18
Q

During gastrulation, epiblast cells undergo what transition, causing them to lose their cell-to-cell adhesion properties

A

Epithelial-to-mesenchymal

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19
Q

The anterior pituitary is derived from what structure, which is an evagination of the surface ectderm that lines the fetal oral cavity

A

Rathke pouch

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20
Q

The posterior pituitary is derived from what embryonic cells

A

Neuroectoderm

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21
Q

The posterior pituitary is derived from the ______ which is an extension of neuroectoderm from the diencephalon

A

Infundibulum

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22
Q

What is the condition characterized by a sudden, involuntary contraction of a major muscle group that developes within 4 hours and 4 days of starting an antipsychotiv medication

A

Acute dystonic reaction

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23
Q

What is the presentation of dystonia as a oculogyric crisis

A

Forced, sustained elevation of the eyes in an upward position

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24
Q

How does opisthotonus (a dystonic reaction) present

A

Arching of the back with the head thrown backward

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25
Q

How does spasmodic torticollis (a dystonic reaction) present

A

Pain and stiffness on one side of the neck

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26
Q

Acute dystonic reactions a theorized to result from the antipsychotic property of D2 antagonism in what pathway

A

Nigostriatal

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27
Q

Dopamanergic blockade causes excess _____ _activity in the striatum leading to extrapyramidal side effects

A

Cholinergic (M1)

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28
Q

L5 radiculopathy presents with sensory loss where?

A

Lateral thigh
Calf
Dorsal foot

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29
Q

L5 radiculopaty often presents with weakness where?

A

Great toe extension

Foot dorsiflexion, inversion, and eversion

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30
Q

What is pleocytosis in a CSF sample

A

Elevated leukocyte count

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31
Q

What bacteria has distinctive tumbling motililty at room temperature

A

Listeria monocytogenes

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32
Q

How is listeriosis most commonly transmitted in adults

A

Food ingestion (can replicate in cold (refrigerator)

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33
Q

Listeriosis can have what presentation in immunocompromised adults

A

Meningitis

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34
Q

Migraines are associated with cortical spreading depression and subsequent stimulation of _____ afferents in the meninges causing release of vasoactive neuropeptides

A

Trigeminal

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35
Q

Trigeminal aferents in the meninges cause release of vasoactive peptides including substance P and __________, resulting in neurogeninc inflammation, vasodilation, and plasma protein extravasation which can casue migranes

A

Calcitonin gene-related peptide (CGRP)

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36
Q

Triptans, such as sumatriptan, are ________ agonists that directly counter migraine hedaches by binding trigeminal ____ receptors and inhibiting CGRP release from trigeminal neurons

A

Sertonin 5-hydroxytryptamine 1B/1D

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37
Q

Triptans bind serotonin recepotrs on smooth muscle cells of blood vessels and result in intracranial ____

A

Vasodilation

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38
Q

Tryptans are commonly prescribed as ______ therapy for acute migraines, particularly in patients who are not responsive to analgesics

A

Abortive

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39
Q

Significant adverse effects of triptans (used aas migrain therapy) include dizziness, chest tightness, and _____

A

Hypertension

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40
Q

The extracranial portion of the facial nerve exits the skull via ______ foramen

A

Stylomastoid

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41
Q

Where does CN VII divide into 5 terminal branches

A

Within the parotid gland

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42
Q

Parotid gland tumors can compress and disrupt the ipsilateral facial nerve and its branches leading to _____

A

Facial droop

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43
Q

Parotid gland tumors that cause facial nerve paralysis are often ______

A

Malignant

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44
Q

Tetanospasmin (potent metalloprotease exotoxin) inhibits release of what neurotransmitters

A

Glycine and gamma-aminobutyric acid (GABA)

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45
Q

What is the term for lockjaw seen in C.tetani infections

A

Trismus

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46
Q

What is the term for the contractions of back muscles resulting in backward acing seen in infections with C. Tetani

A

Opisthotonos

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47
Q

all 3 opiate receptor subtypes are transmemrane receptors that are coupled to ____ G proteins

A

Inhibitory

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48
Q

Which opiate recepter exerts the strongest analgesic effects

A

Mu

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49
Q

What effects do opiates have when binding to mu receptors on the primary afferent neurons

A

Closure of voltage gated calcium channels –> reduced calcium influx –> decreased excitatory neurotransmitter release from presynaptic terminal

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50
Q

What effects do opiates binding on mu rceptors on the postsynaptc membrane have

A

Opens potassium channels –> potassium eflux –> hyperpolarization

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51
Q

Dopamine agonists in treating Parkinson disease can result in what behavior change

A

Impulse control disorders

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52
Q

Dopamine agonists, treatment for parkinsons disease, act by binding central dopamine receptors and stimulating dopamine activity in the _____ and substantia nigra

A

Ventral striatum

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53
Q

Where is the nucleus accumbens located

A

Ventral striatum

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54
Q

Nucleus accumbens is involved in motivation and the _____ pathways

A

Reward

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55
Q

Zolpidem is a short-acting nonbenzodiazepine ___ agent

A

Hypnotic

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56
Q

Mechanism of action for zolpidem

A

Bind GABAa receptor at benzodiapine receptor site and act as GABAa agonist

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57
Q

What differs nonbenzodiazepines such as zolpidem from benzos

A

More specific binding –> primarily hypnotics and do not produce anxiolytic, muscle relaxant, o anticonvulsant effects

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58
Q

Campylobacter jejuni causes guillain barre syndrome via immune mediated polyneuropathy due to _________

A

Cross-reacting antibodies (molecular mimicry

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59
Q

In guillain barre syndrome an antecedent event (typically infection) provokes an immune response that cross reacts with the ______ and ______ of peripheral nerves

A

Schwann cells and myelin sheath

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60
Q

Underlying etiology of temporomandibular disorder (TMD) is multifactoral but includes tempromandibular joint(TMJ) derangement and hypersensitivity of the _______ nerve

A

Mandibular

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61
Q

The mandibular nerve is the largest branch of what nerve

A

Trigeminal nerve (it is CNV3)

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62
Q

The mandibular nerve supplies sensation to the TMJ, floor of mouth, ______ tongue and lower part of the face

A

Anterior

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63
Q

The mandibular nerve innervates the muscles of mastication, tensor veli palatini, and ________ which is in the middle ear and dampens loud sounds by tensing the tympanic membrane

A

Tensor tympani

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64
Q

Where does te herpes simplex virus 1 most commonly lay dormany

A

Neural sensory ganglia of trigeminal nerve

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65
Q

During reactivation HSV particles rely on anterograde axonal transport, carried out by ________, to reach the skin and oral mucosa

A

Kinesin

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66
Q

What motor protein, moves intracellular cargo via retrograde axonal transport

A

Dynein

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67
Q

What are two ways that critical illness can cause neuromuscular weakness

A

Critical illness myopathy (atrophy of myofibers)

Critical illness polyneuropathy (axonal degeneration)

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68
Q

What is the cause of cavernous sinus thrombosis

A

Contiguous spread of an infection from the medial third of face, siuses, or teeth

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69
Q

Methylmalonic acidemia results from complete or partial deficiency fo the enzyme ________

A

Methylmalonyl-coA mutase

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70
Q

In methylmalonic acidemia, a methylmalonyl-CoA mutase deficiency, results in a metabolic acidosis and what blood glucose status

A

Hypoglycemia

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71
Q

Why is there an anion gap metabolic acidosis present in methylmalonic acidemia (a deficiency in methylmalonyl CoA mutase)

A

Hypoglycemia –> increased FFA metabolism –> ketones –> anion gap

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72
Q

Why is there hyperammonemia in methylmalonic acidemia

A

There is a build up methylmalonic acid and propioinic acid. Organic acids directly inhibit urea cycle –> hyperammonemia

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73
Q

How is a diagnosis of methylmalonic acidemia confirmed

A

Elevated urine methylmalonic acid and propionic acid

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74
Q

Propionic acidemia is due to deficiency in what enzyme

A

Propionyl CoA carboxylase

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75
Q

How do the lab findings in propionic acidemia differ from methylmalonic acidemia

A

Will not have elevated levels of urine methylmalonic acid

Both have hyperammonemia, hypoglycemia, metabolic acidosis

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76
Q

Axillary nerve originates from the ____ cord of brachial plexus

A

Posterior

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77
Q

Axillary nerve carries fibers from what spinal nerves

A

C5, C6

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78
Q

What is the motor inervation of the axillary nerve

A

Deltoid and teres minor

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79
Q

What is the sensory inveration of the axillary nerve

A

Skin over lateral shoulder

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80
Q

What nerve injury leads to sensory loss over upper later arm and weakness on shoulder abduction due to denervation and possible atrophy of the deltoid muscle

A

Axillary nerve

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81
Q

kinesin is a microtubule associated motor protein whose funciton is anterograde transport of intracellularvesicles and organells toward the ____ end of microtrubules

A

Plus (rapidly growing)

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82
Q

What is the most common cause of cerebellopontineangle (betwen the cerebellum and lateral pons) tumors in adults

A

Vestibular schwannoma

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83
Q

Spontaneous vestibular schwannomas are usually unilateral, whereas bilateral vestibular schwannomas are associated with ___________

A

Neurofibromatosis type 2

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84
Q

What 3 nerves are in proximity at the cerebellopontine anlgle and therefore at risk of being compressed by a vestibular schwannoma

A

VII (facial)
V (trigeminal)
VIII (vestibularcochlear)

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85
Q

What common manifestation of multiple sclerosis is characterized by monocular visual loss with pain on eye movement and an afferent pupillary defect

A

Optic neuritis

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86
Q

MRI findings in _________ typically include white matter lesions scattered throughout the brain and/or spinal cord with a predilection for the subcortical periventricular regions

A

Multiple sclerosis

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87
Q

The pathogenesis of MS involves an autoimmue response targeting ________

A

Oligodendrocytes

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88
Q

Most patients with MS have ______ immunoglobulin bands in the cerebrospinal fluid

A

Oligoclonal

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89
Q

The auto-immune response in multiple sclerosis is __________ mediated

A

T cell and antibody

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90
Q

List the abortive medications use in migraine therapy

A

Triptans (sumatriptan)
NSAIDs, acetaminophen
Antiemetics (metoclopramide, prochlorperazine)
Ergotamine

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91
Q

List the preventative medications used for migraine therapy

A

Anticonculsants (topiramate or valproate)
Beta blockers (metoprolol, propranolol)
Antidepressents (tricyclic: amitrptyline, or venlafaxine)

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92
Q

What age group is almost exclusived affected by febrile seizures

A

6 mo - 5 years (seizure threshold is lower during early years of brain development)

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93
Q

What is the treatment for most febrile seizures

A

Antipyretics (NSAID)

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94
Q

Botulinum toxin prevents the presynaptic release of _____ from the nerve terminal at the neuromuscular junction

A

Acetylcholine

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95
Q

Clostridium botulinum spore formation occurs at _______ location which allows the bacteria to survive adverse conditions such as heat and high oxygen enironments

A

Subterminal (between the terminal end and center of the bacteria)

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96
Q

Injection of _____ into the a dystonic muscle results in muscular relaxation and relief of symptoms

A

Botulinum toxin type B

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97
Q

What is hydrocephalus ex-vacuo

A

Normal CSF expansion following cerebral volume loss rather than abnormal CSF accumulation as seen in hyrdrocephalus

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98
Q

Infants with hydrocephalus typically develop macrocehaly, poor feeding and what two other musculoskeletal/neural findings

A

Muscle hypertonicity

Hyperreflexia

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99
Q

In hydrocephalus, Hypertonicicty and hyperreflexia result from upper motor neuron injury caused by stretching of the ________ tracts

A

Periventricular pyramidal

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100
Q

Treatment of hydrocephalus requires ________

A

Surgical placement of a shunt

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101
Q

Infants with hydrocephalus will show what on imaging

A

Enlarged ventricles

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102
Q

What is the characteristic presentation of paralysis in a patient with botulism

A

Symetric, descending paralysis that first manifests with cranial nerve abnormalities: 3 D’s: diplopia, dysphagia, dysphonia

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103
Q

How does the botulinum toxin prevent the release of Acetylcholine

A

Destroys SNARE proteins

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104
Q

Transected nerves udergo __________ which involves axonal dissolution while activated schwann cells and macrophages degrade myelin

A

Wallerian degeneration

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105
Q

In addition to clearing cellular debris, ______ and macrophages stimulate formaiton of a growth cone from te proximal axon stump to facilitate nerve regeneration

A

Schwann

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106
Q

If regenerating axons cannot find their distal target, regeneration can result in formation of a disroganzed mass of axonal processes, Schwann cells, vascular hyalinization, and fibrosis know as a _______

A

Neuroma

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107
Q

Chronic axonal injury or inflammation induces increased expression of ___________ chanels

A

Voltage gated sodium chanels

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108
Q

To supportthe diagnosis of a neuroma, _______, is administered which will often provide immediate relief of pain

A

Local anesthetic (blocks sodium channels in the neuronal cell membrane –> prevents depolarization of the nerve)

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109
Q

What are the preferred anticonvulsants for focal onset seizures

A

Carbamazepie
Lamotrigine
Levetiracetam
Phenytoin

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110
Q

What anticonvulsants are prefered for tonic-clonic and myoclonic seizures

A

Leveltiracetam

Valproic acid

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111
Q

What are the preffered anticonvulsants for absence seizures

A

Ethosuxamide

Valproic acid

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112
Q

What typically presents in adolscents with brief, involuntary jerking movements involving both upper extremities with preservation of consciousness and symptoms usually occring within the first hour of waking and can be provoked by sleep deprivation

A

Juvenille myoclonic epilepsy

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113
Q

Individuals who consume more than 10 times the daily value of ______ are prone to developing toxicity and may suffer hepatic injury so severe as to cause cirrhosis

A

Vitamin A

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114
Q

Signs and symptoms of acute vitamin A toxicity occur after ingestion of a single high dose of vit A and include:

A

Nausea, vomitting, vertigo and blurred vision

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115
Q

Sings and symptoms of chronic vitamin A toxicity occur after the long-term ingestion of high doses of vit A and include:

A
Alopecia
Dry skin
Hyperlipidemia
Hepatotoxicity
Hepatosplenomegly
Visual difficulties
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116
Q

The cerebellar hemispheres are primarily responsible for _______ of the ipsilaeral extremities

A

Motor planning and coordination

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117
Q

Lesions in the left cerebellar hemisphere typically result in left ________(impaired rapid alternating movements), _______ (overshooting/undershooting during targeted movement), and ________ tremor

A

dysdiadochokinesia
Limb dysmetria
Intention tremor

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118
Q

The cerebellar vermis modulates _____ via connections with the medial descending motor systems

A

Axial/truncal posture and coordination

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119
Q

Vertigo and nystagmus may occur due to disruption of what regions of the cerebellum

A

Inferior vermis and flocculonodular lobe

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120
Q

Mechanism of action: triptans

A

Serotonin 1B/1D agonist

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121
Q

Mechanism of action: metoclopramide

A

Dopamine recepor blocker

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122
Q

Dopamine receptor blockers have both antiemetic and anaglesic effects on migraine headaches by antagonizing central dompamine ____ receptors in midbrain and striatum

A

D2

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123
Q

Dopamne receptor bloackade in teh basal ganglila can cause excess ______ activity that manifests as significant extrapyramidal symptoms such as acute dystonic reaction

A

Cholinergic

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124
Q

What can be co-administered with metoclopramide or prochlorperazine to prvent extrapyramidal symptoms

A

Diphenhydramine (anticholinergic)

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125
Q

________ presents with vague lower extremity discomfot and an urge to move the legs that worsens at night

A

Restless leg syndrome

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126
Q

Causes of restless leg syndrome include idiopathic and 3 others:

A

Iron deficiency
Uremia
Diabetes (especially with neuropathy)

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127
Q

Pathophysiology of restless leg syndrom is not completely understood by likely involves CNS iron deficiency (even in patients with normal serum iron levels) and abnormalities in _______ transmission

A

Dopaminergic

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128
Q

Treatment of restless leg syndrome includes avoidance of aggravating medications, iron replacement, and ________

A

Dopamine agonists (ropinirole, pramipexole)

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129
Q

Characterisc pathologic changes associated with alzheimer disease involve acumulation of intracellulr ______ and extra cellular ______ plaques

A

Neurofibrillary tangles

Amyloid beta

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130
Q

Neurofibrillary tangles are composed of _____ protein, a primary component of intracellular microtubules

A

Tau

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131
Q

In alzheimer disease, tau protein is _____ causing microtubule structures to collapse into “tangles” that contribute to global neuronal dysfunction

A

Hyperphosphorylated

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132
Q

Amyloid beta is an abnormal fragment of ________ protein, which is normally involved in synaptic formation and repair

A

Amyloid precursor protein

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133
Q

An extra copy of ____ gene, located on chromosome 21, present in trisomy 21, is thought to lead to early onset alzheimers disease

A

APP (amyloid precursor protein)

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134
Q

______ phenomenon describes what patients with parkinson disease being treated with levodopa experience in terms of periodc flucuations in motor function

A

“On-off”

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135
Q

As parkinson disease progresses, the therapeutic windo for levodopa narrows, possibly due to natural or levodopa induced ______ degeneration

A

Nigrostriatal

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136
Q

In advanced PD, motor fluctuations can occur independently of dosing and may become _______

A

Unpredictable

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137
Q

A patien who developes prolonged muscle weakness after receiving succinylcholine could have _____________ deficiency, an autosomal recessive disorder caused by a genetic polymorphism in the BCHE gene

A

Pseudocholinesterase deficiency

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138
Q

Psuedocholinesterase deficiency is an autosomal recessive disorder caused by a genetic polymorphism in the _____ gene

A

BCHE

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139
Q

Succinylcholine is a _______ neuromuscular blocking agentused to induce skeletal muscle relaxation during intubation and surgery

A

Depolarizing

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140
Q

Succinylcholine acts as a _________ of nicotinic acetylcholine receptors of the motor endplate, where it induces persistent depolarization, leading to desensitization and skeletal muscle paralysis

A

Competitive agonist

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141
Q

Succinulcholine is rapidly hydrolyzed by plasma ________, only around 10% of the administered dose reaches the neurmuscular junction, where it typically has a duration of action of < 10 min.

A

Pseudocholinesterase

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142
Q

What is another name for neurofibomatosis type I

A

Recklinghausen disease

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143
Q

Neurofibromatosis type I is an autosomal dominant neurocutaeous disorder caused by mutations in _______ gene

A

NF1 (tumor supressor)

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144
Q

In neurofibromatosis type 1, patients typically develop _____ over the trunk

A

Cage au lait spots (hyperpigmented macules)

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145
Q

Patients with neurofibromatosis type I are at increased risk of developing ______ which can cause elevated intracranial pressure and headache

A

Central nervous system neoplasms (optic gliomas, pilocytic astrocytomas)

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146
Q

Cutaneous neurofibromas usually manifest during early adolescence as multiple, raised, fleshy tumors that often increase in size and number with age. These are benign sheath neoplasms predominantly comprised of _____ cells which are embryologically derived from _______

A

Schwann cells

Neural crest

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147
Q

Absence seizures are characteristically provoked by ______

A

Hyperventillation

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148
Q

Treatment for absence seizures

A

Ethosuximide (or valproate if first line is not tlerated or inneffective)

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149
Q

Absence seizures show _____ on electroencephalogram

A

3 Hz spike wave

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150
Q

Mechanism of action of ehosuximide

A

Inhibits T type calcium channels in thalamic neurons

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151
Q

A patient with sudden-onset confusion, memory loss, and anterograde amnsia that resolves in a couple hours is consistent with what dagnosis

A

Transient global amnesia

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152
Q

Risk factors for transient global amnesia

A

History of migraine

Older age

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153
Q

Transient global amnesia is likely due to dysfunction of what area of the brain which is responsible for formation of new memories

A

Hippocampus

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154
Q

When testing the plantar reflex, what action of the patients foot is a positive babinski sign

A

Dorsiflexion with or without fanning of the toes

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155
Q

Babinski signs indicates a _______ motor neuron lesion

A

Upper

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156
Q

Upper motor neuron injury can occur anywhere proximal to _____

A

The anterior hor

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157
Q

A sign of UMN injury includes _____reflexia, _____ paralysis, and ____ muscle tone

A

Hyper
Spastic
Increased

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158
Q

Describe clasp- knife rigidity

A

Increased muscle tension with sudden release on passive flexion

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159
Q

Clasp knife rigidity is present in ____ motor neuron lesions

A

Upper

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160
Q

In pyramidal weakness, a sign of upper motor neuron injury, weakness is more pronounced in lower extremity ______ and upper extremety ______

A

Flexors

Extensors

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161
Q

Pronator drift, due to upper extremity supination being weaker than pronation, is a sign of a ________ motor neuron lesion

A

Upper

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162
Q

Lower motor neuron lesion signs include ____ _paralysis, _______ tonia, and _____ reflexia

A

Flaccid
Hypo
Hypo (or absent)

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163
Q

Fasciculations are present in ___ motor neuron lesions

A

Lower

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164
Q

Histology of guillain barre syndrome demonstrates an inflammatory infiltrate located within the ______

A

Endoneurium (innermost layer of connective tisue that surrounds a nerve axon adn its corresponding blood vessels)

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165
Q

In guillian barre syndrome, macrophages strip the myelin sheath from the axon, and ________ macrophages are seen following the engulfment of myelin

A

Lipid laden

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166
Q

The speed of conduction down an axon depends on what two constants

A

Length (space) constant

Time constant

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167
Q

Myelin _____ the length constant by reducing charge dissipation across the membrane

A

Increases (allows the electrical impulse to propagate further without requiring active regeneration by ion channels)

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168
Q

Myelin ____ the time constant

A

Reduces (allows membrane potential to change faster)

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169
Q

Unilateral hand pain and numbness, thenar atrophy, and weakness of thumb opposition is characteristic of ________

A

Carpal tunnel syndrome

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170
Q

The carpal tunnel is an antaomic space in the wrist between the carpal bones and the ______

A

Transverse carpal ligament (flexor reinaculum)

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171
Q

What structures run through the carpal tunnel

A

Median nerve

9 tendons: flexor digitorum superficialis and profundus, flexor pollicis longus

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172
Q

If carpal tunnel syndrome is not treatable with wrist splints and glucocorticoid injection, surgical decompression can be performed by making a longitudial incision of the ______

A

Transvers carpal ligament

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173
Q

What role do the pili on the capsular surface of N meningitidis have?

A

Attachment to and colonization of the nasopharyngeal epithelium as well as bacterial movement and epithelial penetration

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174
Q

What is the role of Opa-proteins in N. Meningitidis

A

Aid in endothelial attachment and invasion

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175
Q

What virulence factor aids N. Meningitidis by destroying mucosal antibodies that would otherwise inhbit epithelial colonization

A

IgA protease

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176
Q

Capsulr polysaccharides provide what benefit to bacterial organisms (including N. Meningitidis)

A

Prevent phagocytosis and phagolysisime destrution

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177
Q

Why are pili in N. Meningitidis a difficult target for vaccines

A

Significant antigenic variations

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178
Q

What nerve courses along the pericardium and overlies hte right atrium puting it at high risk during procedures that target structures in or near the right atrum

A

Right phrenic nerve

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179
Q

How can an injury to the right phrenic nerve be visualized on a chest xray

A

Elevation of the right (ipsalteral) hemidiaphragm

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180
Q

A patient with history of A fib presenting with isolated left lower extremety motor deficits, most likely had a carioembolic stroke in what artery

A

Right anterior cerebral artery

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181
Q

Occlusion of the ACA characteristically causes contralateral _____ limb weakness and _____ motor neuron signs

A

Lower

Upper

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182
Q

Atrial thromemboli traveling to and obstructing the middle cerebral artery characteristically has contralateral _____ extremity weakness and _____ deficits

A

Upper

Face

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183
Q

Portion of the hypothalamus that mediates satiety, and lesions –> hyperphagia

A

Ventromedial

Ventromedial injury makes you very massive

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184
Q

Portion of hypothalamus that mediates hunger, lesion –> anorexia

A

Lateral

Lateral injury makes you lean

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185
Q

Portion of hypothalamus that mediates heat dissipation, lesion –> hyperthermia

A

Anterior

A/C = Anterior cooling

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186
Q

Portion of hypothalamus that mediates head conservation, lesion –> hypothermia

A

Posterior

Heating controled by posterior= hot pot

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187
Q

Portion of hypothalamus that secretes dopamine (inhibits prolactin) and GHRH

A

Arcuate

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188
Q

Portion of hypothalamus that secretes GnRH and regulates sexual behavior

A

Medial preoptic

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189
Q

Portion of hypothalamus that secretes oxytocin, CRH, TRH, and small amounts of ADH

A

Paraventricular

POX = paraventricular = oxytocin

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190
Q

Portion of hypothalamus that secretes ADH and small amounts of oxytocin

A

Supraoptic

SAD= supraoptic = ADH

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191
Q

Portion of the hypothalamus that regulates circadian rhythm and pineal gland function

A

Suprachiasmatic

SCN is Sun Censing Nucleus

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192
Q

Musculocutaneous nerve roots

A

C5-C7

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193
Q

Musculocutaneous nerve arises from ____ cord of brachial plexus

A

Lateral

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194
Q

Motor innervation of the musculocuaneous nerve

A

Forearm flexors adn corachobrachialis

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195
Q

Sensory innervation of musculocutaneous nerve

A

Lateral forearm

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196
Q

Brown sequard syndrome (result of a spinal cord hemisection) will produce _____lateral paralysis, _____ lateral loss of vibration, proprioception, and light touch, and ____ lateral loss of pain and temperature sense

A

Ipsilateral paralysis
Ipsilateral vibration
Contralateral pain/temp

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197
Q

If a patient fails the romberg test with eyes open then they have ____ ataxia

A

Cerebellar

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198
Q

If a patient is steady during the romberg test with eyes open but fails when eyes are closed they have _____ ataxia

A

Sensory (loss of proprioception)

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199
Q

Tabes dorsalis causes sensory ataxia due to what infection

A

Syphilis

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200
Q

Over 95% of glioblastoma cases are associated with the overexpression of _________ on the surface of neoplastic cells

A

Epidermal growth factor (EGRF)

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201
Q

Mechanism of action: erlotinib

A

Inhibits EGFR/EGFR-ligand interaction

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202
Q

A biopsy of a tumor with hypercellular white matter with extensiveastrocytic aberration, microvascular proliferation and areas of necrosis lined with tumor cells will have what diagnosis

A

Glioblastoma

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203
Q

Right arm numbness and paresthesia caused by a focal onset seizure originates in the ____ side ____ central gyrus

A

Left
Post
(Primary somatosensory cortex)

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204
Q

Wernicke korsakoff syndrome is a complication of ______ defciency and most commonly occurs in patients with history of long standing alcohol abuse or other forms of malnurishment

A

Thiamine (B1)

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205
Q

Thiamine is a vitamin cofactor involved in ____ metabolism and decifiecy resultsin neuoronal damage and necrosis

A

Glucose

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206
Q

Iatrogenic wernike korsafoff an be precipitaed by the administration of ________

A

Glucose containing fluids which depletes the last remianing stores of thiamine

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207
Q

Areas of the brain with high metabolic demand are particularly susceptible to wernicke korsakoff syndrome, focal hemorrhage and atrophy of _______ is characteristic

A

Mammillary bodies

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208
Q

Neurofibromatosis type 1 gene mutation is located on chromosome ___ while NF2 gene mutation is located on chromosome ____

A

17

22

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209
Q

NF1 is a tumor supressor gene that codes _____

A

Neurofibromin

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210
Q

NF2 is a tumor supressor gene that codes protein ____

A

Merlin

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211
Q

Von Recklinghausen disease is associated with what gene mutation

A

NF1 (neurofibromatosis type 1)

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212
Q

Central neurofibromatosis is associated wiith what gene mutation

A

NF2 (neurofibromatosis type 2)

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213
Q

What are the main clinical features of neurofibromatosis type 1

A

Cafe au lait spots
Multiple neurofibromas
Lisch nodules

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214
Q

What are the main clinical features of neurofibromatosis type 2

A

Bilateral acoustic neuromas

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215
Q

A brain tumor causing cerebellar symptoms with sheets of primitive cells with many mitotic figures indicates what diagnosis

A

Medulloblastoma

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216
Q

Primitive neuroetodermal tumors are composed of sheets of small cells with deeply ____ nuclei and ____ cytoplasm

A

Basophilic

Scant

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217
Q

Primitive neuroectodermal tumors are well or poorly differentiated? And good or bad prognosis?

A

Poorlydifferentiated

Poor prognosis

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218
Q

Syringomyelia presents with loss of pain and temperature sensation in the arms and hands due to a fluid filled cavity called a _______ that damages the ________ and sometiems the ventral horns

A

Syrinx

Ventral white commissure

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219
Q

The ventral whitecommissure is the area of decussation for the fibers of the ____ tract

A

Lateral spinothalamic

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220
Q

Axons of the spinothalamic tract briefly ascend in the zone of ____ before decussating

A

Lissauer

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221
Q

The anterior 2/3 of the spinal cord is perfused by the ______ which receives blood flow form segmental arteries arising from te ______

A

Anterior spinal artery

Thoracic aorta

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222
Q

In an anterior cord syndrome how do initial changes in motor fuction progress

A

Initially: flaccid paralysis from spinal shock

Upper motor neuron signs devlop (spasticity, hyperreflexia) over days to weeks

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223
Q

Neoplastic spinal cord compression most commonly results from local extension of vertebral metastases into the ______ space

A

Epidural

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224
Q

Characteristic CT findings of ischemic stroke 6-12 hours after onset of inschemic injury include _____ of the tissue and loss of _____ differentiation within affected region

A

Hypoattenuation

Grey-white matter

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225
Q

Signs of irreversible damage during the first 24 hours after injury in ischemic stroke are ____ (microscopic finding)

A

Red neurons

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226
Q

Neutrophils move into area of ischemic stroke ____ following injury and microglial cells _____ after onset of injury

A

1-2 days

3-7 days

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227
Q

_______ is the product of neuron disintegration and microglia phagocytosing their fragments which along w myelin breakdown products accumulate in the microglia cytoplasm

A

Foamy lipids

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228
Q

In Guillain barre syndrome, ______ demyelination and an _____ inflammatory infilttrate composed of lymphocytes and macrophages are seen on light microscopy

A

Segmental

Endoneurial

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229
Q

Fragile X syndrome mode of inheritence

A

X linked

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230
Q

Fragile x syndrome is an x linked disorder caused by ____ mutation in hat gene

A

Loss of function

Fragile x mental retardation 1 (FMR1)

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231
Q

Which arm of the x chromosome is the FMR1 gene located

A

Long arm

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232
Q

Presentation of _______ includes long, narrow face, prominent forehead and chin, large testes, hyperlaxity of joints, developmental delay, and neuropsychiatric features

A

Fragile x syndrome

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233
Q

Anxiety and agnitation are central effects of dopamine and are caused by what parkinson disease treatment

A

L-dopa

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234
Q

Why might adding carbidopa to L-dopa treatment worsen anxiety and agitation side effects

A

Carbidopa inhibits peripheral conversion of levodopa, making more of it availible to the brain

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235
Q

How long following an ischemic stroke do red neurons with eosinophiliccytoplasm, pyknotic nuclei and loss of Nissl substance appear

A

12-24 hours

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236
Q

How long following an ischemic stroke does neutrophilic infiltration occur

A

24-72 hours

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237
Q

How long after a stroke do macrophage/microglia innfiltratation and phagocyosis begin

A

3-7days

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238
Q

How long after an ischemic stroke does reactive gliosis and vascular proliferation around he necrotic area occur

A

1-2 weeks

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239
Q

How long afer an ischemic stroke does a glial scar form

A

> 2 weeks

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240
Q

How long after an ischemic stroke does liquefactive necrosis occur

A

1 wk-1 month

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241
Q

How long after an ischemic stroke does a cystic area surrounded by dense glial fibers form

A

> 1 month

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242
Q

Why might someone exposed to organophosphates experience wheezing

A

Cholinesterase inhibitor –> cholinergic overstimulation –> bronchospasms

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243
Q

In viral meningitis, CSF will have a WBC count of ______ with ______ cell predominance

A

<500

Lymphocytic

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244
Q

In viral meningitis, glucose levels are _____ and protein levels are _____

A

Normal or slightly reduced

<150

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245
Q

In CSF of viral meningitis, CSF gram stain/culture will have what result

A

No organsism identified

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246
Q

In bacterial meningitis, CSF WBC count is ______ with _____ cell predominece

A

> 1000

Neutrophilic

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247
Q

In bacterial meningitis, the CSF has glucose levels of ______ and protein is _______

A

<45

>250

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248
Q

A CSF gram stain in bacterial meningitis will often have what result

A

Positive for a specific organism

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249
Q

What is the most common viral cause of meninitis

A

Enterovirus (>90%)

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250
Q

What virus can present with the following clinical signs: fever, headache, rash, meningitis, echphalitis, acute asymmetric flaccid paralysis, parkinson symptoms

A

West nile virus

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251
Q

West nile virus is a _____ sense _____ stranded RNA virus

A

Positive

Single

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252
Q

Who is at risk for a west nile virus becoming neuroinvassive

A

Older
Malignancy
Organ transplant

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253
Q

What may be suspected of a patient with oral thrush and cervial and inguinal lymphadenopathy

A

HIV

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254
Q

Headache, seizures, multiple ring enhancing central nervous system lesions in a patient with HIV indicates what diagnosis

A

Toxoplasmic encephalitits

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255
Q

List two modes of transission for tocoplasmic encephalitits

A
Extensive pet (cat)exposure
Contaminated food
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256
Q

Neuroleptic malignant syndrome is a life threatening adverse effect due to block of _____ receptors in the brain

A

Dopamine

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257
Q

If a patient who recently started using an antipsychotic presents with fever, confusion, muscle rigidty, and autonomic instability (abnormal vital signs, sweating) what might they be experiencing

A

Neuroleptic malignant syndrome

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258
Q

Mechanism of action: dantrolene

A

Atnagonizes ryanodine receptors and inhibits calcium release from sarcoplasmic reticulum

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259
Q

____ of inhaled anesthetic is inversly proportional to the minimal alveolar concentration

A

Potency

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260
Q

The minimal alveolar concentration referes to the percentage of anesthetic in the inspired gas mixture that renders ____ of patients unresponsive to painful stimulil

A

50%

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261
Q

What nerve innervates all of the extensor muscles of the upper limb below the shoulder and provides sensory inervation to the skin of the posterior arm, forear, and dorsal lateral hand

A

Radial

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262
Q

Radial nerve receives fibers from what nerve roots

A

C5-T1

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263
Q

The radial nerve tracks within the radial groove of the humerus, therefore it is vulnerable to tramatic injury at the ______

A

Humeral midshaft

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264
Q

Patients with proximal radial neuropathy typically have weakness during _______ and variable sensory loss over the posterior arm and forearm

A

Wrist and finger extension (wrist drop)

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265
Q

Damage to the proximal radial nerve can occur at the _____ or the midshaft of the humerus

A

Axilla

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266
Q

The blood brain barrier is formed by _____ between nonfenestrated capillary endothelial cells that prevent the paracellular pasage of fluidsand solutes

A

Tight junctions

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267
Q

L-DOPA has low lipid solubility but is able to enter brain due to _______

A

Its high affinity for the large neutral amino acid transporter

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268
Q

Liquefactive necrosis is charcteristic of irreversible CNS injury becuase of the brains high cholesterol content and lack of supporting architecture. It also occurs in other body tissues in the setting of severe infection/inflamation because of the release of _______ from reacting inflammatory cells.

A

Hydrolytic enzymes

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269
Q

How does a nicotinic receptor function

A

Its 2 acetylcholine binding sites must be filled and the ion channel opens, allowing sodium and calcium influx and sodium outflux —> end plate potential

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270
Q

Nitrous oxide is a ____ soluble gas

A

Poorly

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271
Q

A gas that is poorly soluble, such as nitrous oxide, partial pressure will rise rapidly and plateua, indicating that the blood quickly becoems _____with the anesthetic

A

Saturated

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272
Q

Blood solubulity of an anesthetic is indicated by itsblood/gas partition coefficient, anesthetics with a higher blood slubility will have a ______ blood/gas partition coefficent

A

Larger

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273
Q

A gas with higher solubulity (thus a larger blood/gas partition coefficient) will havea partial pressure in blood that rises more _____ than a low solubilty gas

A

Slowly

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274
Q

Poorly soluble gases equilibrate with the brain ______ than highly soluble gases

A

Faster

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275
Q

Poorly soluble gases have a ______ onset than highly soluble gases

A

More rapide

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276
Q

The first pharyngeal arch is associated with what nerve

A

Trigeminal (V)

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277
Q

Bony derivatives of first pharyngeal arch

A
Maxilla
Zygoma
Mandible
Incus
Malleus
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278
Q

Muscle derivatives of first pharyngeal arch

A

Muscles of mastication

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279
Q

Second pharyngeal arcassociated with what nerve

A

Facial nerve (VII)

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280
Q

Second pharyngeal arch gives rise to what bones

A

Styloid process of temporal bone, lesser horn of hyoid, and stapes

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281
Q

Muscles derived from 2nd pharyngeal arch

A

Muscles of facial expression

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282
Q

Treacher collins syndrome is a genetic disorder resulting in abnormal development of _____

A

1st and 2nd pharyngeal arches

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283
Q

Treacher collins syndrome will preset with craniofacial abnormalities resulting in airway compromise and feeding difficulties as well as what other clinical finding

A

Profound conductive hearing loss

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284
Q

The most notable manifestaions of vitamin E deficiency are hemolysis and neurologic dysfunciton due to _____

A

Free radical damage of cell membranes

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285
Q

Neurologic symptoms of vitamin E deficiency closely mimic _______ which include ataxia ue to degeneration of spinocerebellar tracts, loss of position and vibration sense due to degeneration of the dorsal columns and loss of deep tendon reflexes due to peripheral nerve degeneration

A

Friedreich ataxia

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286
Q

Intraventricular hemorrhage in preterm infants usually originates from ______, a highly cellular and vascularized layer in the subventricular zone (source of neurons and glial cells during brain development)

A

Germinal mattrix

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287
Q

The germinal matrix contains numerous fragile, thin walled vessels that lack _____ that support other blood vessels throughout the bain, making them more susceptible to hemorrhage

A

Glial fibers

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288
Q

There is reduced risk of intraventricular hemorrhage in infants born after _____ weeks because the germinal matrix starts to become less prominent and its cellularity and vascularity decreases

A

32

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289
Q

Neonatal intraventricular hemorrhage occurs in infants born before 32 weeks nd/or birth weight

A

1,5000 g (3 lb 5o z)

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290
Q

Creutzfeldt-Jakob disease is a ____ disease: transmissible spongiform encephalopathy

A

Prion

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291
Q

Creutzfeldt-Jakob disease presents in previously healthy patients with ______ dementia associated with ________

A

Rapidly progressive

Myoclonus

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292
Q

Prion diseases are associated with the hange in structural confirmation of ______

A

Prion protein (PrPc)

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293
Q

The abnormal prion protein (PrPsc) in prion diseases is resistant to ______ and accumulates within neuronal and glial cells causing neural cell death

A

Enzymatic degredtion

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294
Q

Histopathology of Creutzfeldt-jakob disease shows widespread neuronal loss with small, uniform ____ in the gray matter of the brain

A

Vacuoles (spongiform encephalopathy)

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295
Q

What form of vaccine is administered for measles virus

A

Live attenuated

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296
Q

Measles genome codes for structural proteins including ____ which mediates cell surface adhesion and ____ which is important for virral assembly

A

Hemagglutinin

Matrix protein

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297
Q

______ is a rare complication of measles that occurs in children or young adults several years after the infection

A

Subacute sclerosing panencephalitis

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298
Q

Subacute sclerosing panencephailtis is caused by a form of measles virus with a mutated or absent _____ protein, allowing the virus to replicate intracellularly, evading the immune system

A

Matrix

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299
Q

Accumulation of measles viral ______ within neurons and oligodendrocytes results in the formation of intranuclear inclusions and eventually leads to inflammation, demyelination, and gliosis in manny cerebral areas (subacute sclerosing panencephalitis)

A

Nucleocapsids

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300
Q

________ of measles virus antibodies are found in the CSF of patients with subacute sclerosing panecephalitis secondary to measles infection

A

Oligoclonal bands

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301
Q

Cognitive decline and chorea along with a family history of similar symptoms are suggestive of what diagnosis

A

Huntingon disease

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302
Q

Huntington disease is due to ______ in the huntington gene leading to a gain of function mutation

A

Excessive number of CAG trinucleotide repeats

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303
Q

In Huntigton disease, the buildup of abnormal/toxic mutant huntingtin protein leads to loss of ____ in what region of the brain

A

Inhibitory GABA neurons

Caudate nucleus

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304
Q

Imaging in a patient with Huntington disease will reveal atrophy of the ___ leading to enlargement of the _____

A

Caudate nuclei

Lateral ventricles

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305
Q

The caudate nucleus and the _____ make up the striatum which is critical for movement control and coordination as well as behavior regulation

A

Putamen

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306
Q

Common manifestations of tabes dorsalis inlude sensory ataxia, absent deep tendon reflexes, and _____

A

Lancinating pains

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307
Q

Spirochetal damage to the midbrain _____ commonly results in Argyll Robertson pupil

A

Tectum

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308
Q

Positive VDRL is diagnostic of what infection

A

Syphilis

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309
Q

Normal aging leads to the following sleep changes: _______ total sleep time, slow wave sleep with _____ nighttime sleep latency

A

Decreased

Increased

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310
Q

What is the cause of isolated anosmia (leading to lack of taste) due to a head trauma

A

Acceleration-deacceleration forces lead to avulsion of olfactory nerve rootlets

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311
Q

A spinal cord disection at C7 would effect maximum insipiration or expiration more?

A

Expiration

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312
Q

Above the splenic flexure, peristalsis is controlled parasympathetic stimulation from what nerve

A

Vegas

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313
Q

Below the splenic flexure, peristalsis is controlled by parasympathetic innervation from what nerve

A

S2-S4 nerve roots

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314
Q

The external anal sphincter is controled by voluntary control (skeletal muscle) whic is innerrvated by what nerve

A

Pudendal nerve (S2-S4)

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315
Q

Decerebrate posture is due to a lesion _____ the red nucleus and results in contraction of the _______ muscles

A

Below

Extensor

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316
Q

Decorticate posture is due to a lesion ____ the red nucleus and results in contraction of the ___ muscles

A

Above

Flexor

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317
Q

Intracranial hemorrhage can cause significant mass effect and increase cranial pressure which can manifest with seizures and_________ triad (hypertension, bradycardia, bradypnea)

A

Cushing

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318
Q

Uncal herniation initially disrupts the ipsilateral occulomotor nerve (CN III) leading to _____

A

Fixed dilated pupil

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319
Q

The _____ tract regulates upper extremity flexor tone and originates from the red nucleii in the rstral midbrain

A

Rubrospinal tract

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320
Q

The rubrospinal tract is ______ by descenfing cortical output from the cerebral cortex

A

Inhibitted

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321
Q

The opthalmic nerve (CN V1) exits the skull through what foramen

A

Superior Orbital fissure then supraorbital foramen

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322
Q

The maxillary nerve (CN V2) exits the skull through what foramen

A

Foramen rotundum then infraorbital canal then infraorbital foramen

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323
Q

The mandibular nerve (CN V3) exits the skull through what foramen

A

Foramen oval

The alveolar nerve branch enters mandibular foramen then exits through mental foramen

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324
Q

what protein has apple green birefringence when stained ith congo red

A

Amyloid

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325
Q

Amyloidosis and Alzheimer disease both show apple green befringence with congo red staind but how do they differ

A

Alzheimer disease amyloid deposits are only seen in brain tissue

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326
Q

Spastic cerebral palsy may be caused by periventricular white matter necrosis which leads to loss of descending _____control from the upper motor neurons

A

Inhibitory

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327
Q

Lack of CNS inhibition leads to hyperactve ______

A

Stretch reflex

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328
Q

In the stretch reflex, muscle lengthening is sensed by _____

A

Muscle spindle

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329
Q

Afferent signal of stretch is conveyed to the spinal cord via the ____ nerve fibers

A

Dorsal

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330
Q

Efferent signals of the stretch reflex are conveyed via the ___ root of the spinal cord

A

Ventral

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331
Q

In the stretch reflex ____ muscle fibers are stimulated, causing muscle contraction

A

Extrafusal

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332
Q

The ___ reflex is responsible for deep tendon reflexes and the maintenacne of muscle tone

A

Stretch

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333
Q

A selective dorsal rhizotomy procedure destroys the ____ arm of the reflex arch, which decreses muscle tone without sacrificing motor innervation of the muscles

A

Afferent (sensory)

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334
Q

Symmetric, bilateral wedge shaped strips of necrosis over the cerebral convexity are characteristic of _____ cerebral ischemia

A

Global

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335
Q

Profound systemic hypotension diminishes blood suply to the entire brain, resulting in neuron cell death in areas that are vlnerable to hypoxia such as _____ and _____

A

Watershed areas and regions with high metabolic demand

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336
Q

______ is a group of hereditary peripheral neuropathies characterized by mutations in genes coding for peripheral nerce axonal or myelin proteins presenting with adolescent lower extremett weakness, muscle atrophy and peripheral neuropathy

A

Charcot marie tooth disease

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337
Q

The most common type of charcot marie tooth (CMT1) occurs due to autosmal dominant mutation in the ______ gene

A

PMP22

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338
Q

Sudden upward jerking of the arm at the shoulder can cause injury to the _____ trunk of the brachial plexus

A

Lower

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339
Q

the lower trunk of the brachial plexus carried nerve fibers from the C8 and T1 spinal levels that ultimately contribute to the ____ and ___ nerves

A

Median and ulnar

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340
Q

Injury to the intrinsic hand muscles leads to ______ palsy: weakness of the lumbricals –> impaired flexion of metacarpophalangeal joints and impaired extension of the interphalangeal joints: claw like deformity

A

Klumpke’s palsy

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341
Q

What nerve exits the brain stem at the lateral aspect of the mid-pons at the level of the middle cerebellar peduncles

A

Trigeminal

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342
Q

What is a key neuroanatomic andmark for locating the trigeminal nerve

A

Middle cerebellar peduncle

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343
Q

Infarcts to the anterior pons can affect the ____ tracts

A

Corticospinal (contralateral hemiparesis)

Corticobulbar (contralateral lower facial palsy, dysarthria)

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344
Q

In an isolated CN III palsy, how is the eye oriented

A

Down and out

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345
Q

What eye muscles are not innervated by CN III

A
Superior oblique (CN IV)
Lateral rectus (CN VI)
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346
Q

Aneurysms causing CN III palsy most often involve the ______ artery

A

Posterior communicating artery

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347
Q

Hydrocepalus (enlargement of the ventricles) caused by central neuronal volume loss (rather than excessive CSF) is called_______

A

Hydrocephalus ex-vacuo

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348
Q

In hydrocephalus ex-vacuo, the CSF pressure is____

A

Normal

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349
Q

In communicating hydrocephalus, CSF flows freely between the ventricles and subarachnoid space but there is decreased CSF absorptionin at the ________

A

Arachnoid granulations

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350
Q

Normal pressure hydrocephalus is _______ while high pressure hydrocephalus is _______

A

Chronic

Acute

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351
Q

A patient with unilateral optic neuritis is most likely to demonstrate an _____ pupillary defect due to demyelination of the right optic nerve

A

Afferent

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352
Q

The optic nerve carries the afferent limb of the puppillary light reflex, transmitting informaiton about light entering the eye to the ______ area in the midbrain

A

Pretectal

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353
Q

The pretectal area activates the ______ nuclei bilaterally which send paraympathetic efferent motor fibers down the oculomotor nerve to innervate the pupillary sphincter muscle to each iris

A

Edinger-westphal

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354
Q

Patients with an afferent pupillary defect will have what effect on pupillary constriction when light s shined in the non affected eye

A

Normal pupillary reflex bilaterally

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355
Q

What is first line therapy for essential tremor

A

Beta blocker (propranolol)

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356
Q

In patients with __________ exposure to certain anesthetic agents such as succinycholine and inhalation gasses causes unregulated passage of calcium form the sarcoplasmic reticulum into the intraacellular space

A

Malignant hyperthermia

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357
Q

In malignant hyperthermia, excessive myoplasmic _____ accumulation results in sustained muscle contraction, which is often first noted in the masseter

A

Calcium

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358
Q

What causes a high temperature in patients with malignant hperthermia

A

Sustained muscle contractions –> ATP consumption –> excessive heat production

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359
Q

Treatment for malignant hyperthermia

A

Dantrolene (blocks further release of calcium into the intracellular space)

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360
Q

Blotchy red muscle fibers on Gomori trichrome stain are characteristic of ________

A

Mitochondrial myopathies

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361
Q

In mitochondrial myopathies, abnormal mitochondria accumulate under the sarcolemma of muscle fibers causing the muscle fibers ro have irregular shape and size on cross section, for this erason mitochondrial myopathies are also known as ______

A

Red ragged fiber disease

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362
Q

Phenytoin is a ______ of p450

A

Inducer

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363
Q

_______ malformations are a group of congential disorders caused by unerdevelopment of the posterior fossa

A

Chiari

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364
Q

Chiari type I is more benign and presents when?

A

Adolescence/adulthood

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365
Q

Chiari tpe II typically presents when

A

Neonatal period

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366
Q

How does chiari type I differ from the herniation seen in chiari type II

A

Chiari type I only has the ccerbellar tonsils below the foramen magnum but chiari type II has downward displacement of the cerebellum and the medulla through the foramen magnum

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367
Q

What complications are common in type two chiari

A

Non communicating hydrocephalus

Lumbar myelomeningocele

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368
Q

Where does VZV lie dormant

A

(Migrates via sensory nerves to) cranial nere and dorsal spinal ganglia

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369
Q

What organism is a round/oval yeast surrounded by thick polysaccharide capsule

A

Cryptococcus neofromans

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370
Q

Cryptococcal diagnosis can be confirmed by cryptococcal antigens in CSF or visualiztion of encapsulated budding yeasts in CSF using what 2 specilized stains

A

India ink

Methenamine silver

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371
Q

Spinal muscular atrophy is caused by mutation in the ______ gene which encodes a protein involved in the assembly of small nuclear ribonucleoproteins (snRNPs)

A

Survival motor neuron gene (SMN1)

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372
Q

Defective snRNP assembly, as seen in spinal muscular atrophy, results in impaired _____ function and degeneration of anterior horn cells in the spinal cord

A

Splicesome

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373
Q

Non-coding RNA differs from other RNA how?

A

They carry out functions without first being translated into proteins

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374
Q

A collection of snRNPs and other proteins on a pre-RNA is referred to as a ____

A

A splicesome

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375
Q

Splicesomes remove ____ from preRNA

A

Introns

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376
Q

Infants with spinal muscular atrophy often have flaccid paralysis due to degeneration of _____ cells in the spinal cord

A

Anterior horn

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377
Q

Long standing rheumatoid arthritis frequntly involvesthe cervical spine and causes joint destruction with vertebral malalignment which is called _______

A

Subluxation

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378
Q

What is concerning about endotracheal intubation with a patient who has long standing rhuematoid arthritis

A

Extension of the neck can worsen subluxation leading to acute compression of the spinal cord and or vertebral arteries

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379
Q

Mechanism of methotrexate

A

Folic acid analog –> inhbits dihydrofolate reductase –> rapidly dividing cells dodnt have DNA synthesis or repair

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380
Q

An MRI with ventriculomegaly without sulcal enlargemnt is characteristic of ____

A

Normal pressure hydrocephalus

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381
Q

Normal pressure hydrocephalus causes lateral entrical expansion –> stretching of _______

A

Descending cortical fibers (corona adiata)

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382
Q

What is the classic triad of normal pressure hydrocephalus symptoms due to stretching of te cortical fibers

A

Dementia, gait disturbance, and urinary incontinence

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383
Q

The micturition reflex is an autononomic spinal reflex that receives inhibition from ____

A

Cerebral cortex

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384
Q

Lack of cortical inhibition on the micturition reflex results in _____ hyperactivity

A

Detrusor (–> urge incontinence)

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385
Q

The stapedius nerve, which innerates the stapes, is a brnch of what nerve

A

Cranial nerve VII (facial)

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386
Q

Paralysis of the stapedius muscle results in ______ (increased sensitivity to sound)

A

Hyperacusis

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387
Q

The pudendal nerve oriinates from ____ nerve roots

A

S2-S4

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388
Q

Pudendal nerve exits the pelvis throught hte ____ foramen

A

Sciatic

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389
Q

Motor branches of the pudendal nerve innervated the _____ and _____

A

Pelvic floor muscles

External urethral and anal sphincters

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390
Q

What is the draw back of using atropine rather than pralidoxime in organophosphate poisoning

A

Atropine is competitive inhibitorat muscarinic receptors only, nicotinic symptoms will persist (muscle paralysis)

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391
Q

How do demyelinating neuropathies differ from axonal neuropathies on a nerve conduction study

A

Demyelinating: delayed nerve conduction velocity
Axonal: reduced signal amplitude

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392
Q

Ulnar neuropathy is characterized by numbness of the _____ digits, pain, and weakness

A

4th and 5th

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393
Q

___ is the most common brain tumor in children and appears as a heterogenous, well-circumscribed cerebellar mass

A

pilocytic astrocytoma

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394
Q

what are the two microscopic findings in a pilocytic astrocytoma

A
glial fibrillary acidic protein (GFAP) positive hairlike processes
rosenthal fibers (eosinophilic intracytoplasmic inclusions)
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395
Q

how can a pilocytic astrocytoma be differentiated from a medulloblastoma

A

presence of both cystic and solid components on imaging

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396
Q

the neural tube is a structure that is connected to the amniotic cavity by opening at the ends know as ____ and ______

A

anterior and posterior neuropores

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397
Q

failure of neuropore closure by 4 weeks gestation leads to _____

A

neural tube defects

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398
Q

anterior nerual tube defects include ____ (absence of forebrain) and _______ (protrusion of neural tissue through the cranial defect)

A

anecephaly

encephalocele

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399
Q

what is the most mild form of a posterior neural tube defect

A

spina bifida occulta

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400
Q

a meningocele and meningomyelocele present as cystic masses at the lower spine that are sometimes covered by a tuft of hair, meningomyelocele has what difference from meningocele though

A
meningocele = meninges protruding
meningomyelocele= meninges and spinal cord or cauda equina protruding
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401
Q

prenantal use of what medication, used for bipolar or epilepsy, is associated with a 10 - 20 fold increased risk for NTD

A

valproate

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402
Q

lamotrigine MOA

A

blocks voltage gated sodium channels

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403
Q

most concerning side effect associated with lamotrigine use

A

stevens johnson syndrome, or toxic epidermal necrolysis

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404
Q

what is the difference between stevens-johnson syndrome and toxic epidermal necrolysis

A

SJS involves <10% of the body and TEN has >30% involvement

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405
Q

presentation of steven johnson syndrome

A

flu like symptoms followed by widespread mucocutaneous epidermal necrosis

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406
Q

the presence of nonreactive pupils to light stimulation following cardiac arrest carries a por prognosis and indicates anoxic damage to the brainstem at the level of ______

A

the upper midbrain

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407
Q

cryptococcus neoformans is a llow virulence yeast with a thick polysaccharide capsule/ . It resides in soil contaminated by bird droppings and human exposure primarily occurs due to inhalation into the ____

A

lungs

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408
Q

first line treatment for trigemnial neuralgia

A

carbamazepine

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409
Q

carbamazepine MOA

A

reduces ability of sodium channels to recover from inactivation

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410
Q

fatigable muscle weakness with restoration of strength after rest, affecting voluntary muscles, particularyl those innervated by motor nuclei of the brain stem characterizes what disease

A

myasthenia gravis

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411
Q

myasthenia gravis is most commonly caused by autoantibodies against _____

A

postsynaptic acetylcholine receptors

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412
Q

in myasthenia gravis, th reduced number of postsynaptic cation channels that can open in response to acetylcholine causes what change to the action potential

A

reduces the amplitude of the motor end plate potential and prevents muscle fiber depolarization

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413
Q

how do tricyclic antidepressents and SNRIs treat neuropathic pain

A

decrease of serotoninc and norepiniephrine reuptake –> inhibition of pain signals

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414
Q

how do anticonvullsants treat neuopathic pain

A

decrease depolarization of neurons in the CNS

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415
Q

how does Capsaicin (topical) treat neuropathic pain

A

loss of membrane potential in nociceptive fibers

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416
Q

how does lidocaine treat neuropathic pain

A

decreased depolarization of neurons in peripheral nerves

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417
Q

MOA of capsaicin

A

activation of TRPV1 (transmembrane cation channel) –> build up of intracellular calcium –> long lasting dysfunction of nociceptive nerve fibers (defunctionalization)
it also causes release and depletion of substance P

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418
Q

monocular scotoma is caused by lesion where

A

partial lesion of retina, optic disc, optic nerve

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419
Q

right anopia is due to a lesion where

A

right optic nerve

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420
Q

bitemporal hemianopia is due to lesion where

A

optic chiasm

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421
Q

right nasal hemianopia is due to lesion where

A

right perichiasmal lesion

422
Q

left homonymous hemianopia is due to lesion where

A

right optic tract or optic radiation

423
Q

left homonymous superior quadrantanopia (pie in sky) is due to what lesion

A

right temporal lobe (meyers loop)

424
Q

left homonnumous inferior uadrantanopia (pie on floor) is due to what lesion

A

right parietal lobe (dorsal optic radiation)

425
Q

left homonumous hemianopia with macular sparing is due to what lesion

A

right primary visual cortex (occipital lobe)

426
Q

what are the results of a compound muscle action potential (CMAP) and high rate repetitive nerve stimulation in a patient with clostridium botulinum

A

decreseased CMAP

improves as rapid depolarization rate increases

427
Q

clostridium botulinum will present with the classic 3 D’s : _____, ____, and ____

A

diplopia, dysphagia, and dysphonia

428
Q

peroxisomes functions include hydrogen peroxide degredation and _____

A

oxidation of very long and branched-chain fatty acids

429
Q

Zellweger syndrome is caused by defective ____ biogenesis

A

peroxisomal

430
Q

x-linked adrenoleukodystrophy is characterized as defective transport of ___ into peroxisomes

A

VLCFAs (very long chain fatty acids)

431
Q

carpal tunnel syndrome is a peripheral mononeuropathy caused by compression of the ___ nerve in the carpal tunnel

A

median

432
Q

fragile x mental retardation 1 gene on the long arm of the X chromosome normally has 5-55 CGG trinucleotide repeats and can potentially expand during ____

A

meiosis in oocytes

433
Q

full mutation in fragile X syndrome is characterized as > _____ CGG repeats which causes FMR1 ________

A

200

hypermethylation

434
Q

what test is done to anylze the degree of methylation

A

southern blot

435
Q

occlusion of the PICA results in lateral medullary syndrome, AKA ____ syndrome

A

wallenburg

436
Q

occlusion of the PICA/wallenburg syndrome results in what 4 symptoms

A
  1. vertigo and nystagmus
  2. ataxia
  3. loss of pain and temp in ipsalateral face and contra body
  4. bulbar weakness
437
Q

a drug that binds to and activates GABA-A receptors will increase the conductance of ___ ions, causing pasive transport down the concentration gradient into the cell interior

.

A

chloride

438
Q

patients with _____ stroke can have both sensory and motor deficits, but most commonly have pure motor weakness affecting the contralateral arm, leg, and lower face as well as clasp knife spasticity, hyperreflexia, and positive babinski sign

A

internal capsule

439
Q

dysfunction to what structure would cause an action tremor that increases as hand reaches target

A

cerebellum

440
Q

a patient with history of bulbar symptoms and limb weakness and evidence of asymetric muscular atrophy is indicative of what diagnosis

A

amyotrophic lateral sclerosis (ALS)

441
Q

what structures are affected in the pathology of amyotrophic lateral sclerosis

A

both upper and lower motor neurons

442
Q

_____ tumors are usually non small cell lung cancers that arise near the superior sulcus

A

pancoast

443
Q

pancoast tumors can compress the ____ which can cause ipsilateral shoulder pain/weakness and can compress the ____ which may lead to Horner’s syndrome

A

brachial plexus

cervical sympathetic ganglia

444
Q

Sympathetic first order neurons are located in the ____, their axons descend through brainstem to C8-T2 where they synapse on second order neurons found in _____ column

A

hypothalamus

intermedial cell

445
Q

second order sympathetic neurons synapse on third order sympathetic neurons in the _________ and then travel to the their target tissues in the face and head

A

superior cervical ganglion

446
Q

In a neural tube defect, amniotic fluid will have high levels of ______ and ______

A
Alpha fetoprotein (AFP)
Acetylcholinesterase
447
Q

What herniation type involves herniation of the cingulate gyrus underneath the falx cerebri –> contralateral leg weakness

A

Subfalcine

448
Q

What type of herniation involves herniation of the uncus under the tentorium cerebelli –> ispalateral dilated and fixed pupil and contralateral hemiparesis and then eventually ipsilateral hemiparesis

A

Uncal

449
Q

What type of herniation involves the caudal displacement of diencephalon and brainstem –> rupture of paramedian basilar artery branches –> bilateral midposition and fixed pupils and decroticate then decerebrate posturing

A

Central

450
Q

What type of herniation involves herniation of th cerebellar tonsils through the foraen magnum –> coma, loss of CN reflexes, flaccid paralysis and respiraatory arrest

A

Tonsillar

451
Q

What is the cause of osmotic demyelination syndrome (central pontine myelinolysis)

A

Overly rapid correction of hyponatremia

452
Q

Clinical features of osmotic demyelination syndrome

A

Quadriplegia
Pseudobulbar palsy
Reduced level of consciousness

453
Q

MRI of osmotic demyelination syndrome shows ____

A

Focal demyelination of the pons

454
Q

What is the syndrome that is X linked recesive and is characterized as dstonia, choreoathetosis, self mutilation, and hyperuricemia withing the first years of life

A

Lesch-Nyhan syndrome

455
Q

Lesch-nyhan syndrome is a condition caused by a deficiency of ______

A

Hypoxanthine-guanine phosphoribosyltransferase (HGPRT)

456
Q

Hypozanthine-guanine phosphoribosyltransferase is an enyzme that normally functions in the purine salvage pathway, and in its absence, ____ levels increase

A

Uric acid

457
Q

Naegleria fowleria can cause primary amebic meningoencephalitis by entering through the ____ during water activities

A

Nasal mucosa (it travels retrograde through the olfactory nerve to the brain)

458
Q

Ethosuximide, the first line treatment for absence seizures, prevents neuronal burst firing by blocking ______

A

Thalamic T-type Ca chanels

459
Q

Mode of inheritence for neurofibromatosis type I

A

Autosomal dominant

460
Q

Neurofibromatosis type 1 is caused by mutation in NF1 gene located on chromosome ___

A

17

461
Q

What are the most common symptoms of neurofibromatosis type 1

A

Cafe au lait spots
Multiple neurofibromas
Lisch nodules (pigmented asymptomatic hamartomas of the iris)

462
Q

VZV lies dormant in the ______ ganglia

A

Dorsal spinal

463
Q

_______ is an incomplete forebrain division into 2 hemispheres with a single lateral ventricle

A

Holoprosecephaly

464
Q

The prosencephalon gives rise to the _____ which develops into the thalamus and third ventricle and the _____ which develops into the cerevbral hemispheres and lateral ventricles

A

Diencephalon

Telencephalon

465
Q

Holoprosencephaly may be due to a variety of factors (ex. Hedsgehog gene mutations), the most common associated chromosomal abnormality is ________

A

Trisomy 13 (Patau syndrome)

466
Q

Early onset familial alzheimer disease is associated with _______ gene on chromosome 21, ________ gene on chromosome 14, and ______ gene on chromosome 1

A

Amyloid precursor protein (APP)
Presenilin 1
Presenilin 2

467
Q

The APP and presenilin gene mutations in early onset alzheimers are thought to promote the production of ______

A

A beta amyloid

468
Q

Late onset familial alzheimer disease is associated with the ____ allele of apolipoprotein E

A

Epsilon 4

469
Q

Regardless of etiology, the initial drug of choice for treating status epilepticus is _______ due to its efficacy and rapid onset of action

A

IV benzodiazepine (lorazepam)

470
Q

Benzodiazepines MOA

A

Allostericly attach to GABA-A receptors causing increased influx of Cl- –> hyper polarization of postsynaptic neuron

471
Q

Diffuse axonal injury, a type of severe traumatic brain injury that can occur from direct blunt force injury or abrupt changes in acceleration-deceleration. The transfer of force can result in immediate shearing of ________ or induce secondary biochemical changes leadgn to degredatin of _____with subsequent ___ breakage

A

White matter tracts
Axonal cytoskeleton
Axon

472
Q

Diffuse axonal injury inhibits normal axonl transport –> accumulation of _____ within axonal swellings at the point of injurry

A

Axonally transported proteins (amyloid precursor, alpha synuclein)

473
Q

Diffuse axonal injury is seen on what imaging

A

MRI (CT may appear normal)

474
Q

Diffuse axonal injury is visible as widespread axonal swelling, most pronounced at the __________

A

Gray-white matter junction

475
Q

West nile virus is enveloped RNA virus that is found in warm climates worldwide. The virus replicates extensively within ___ and is passed to ____

A

Birds

Mosquitos (Culex species)

476
Q

Cryptococcal neoformans can be cultured on ____ agar

A

Sabouraud

477
Q

Initial treatment of cryptococcal meningoencephalitis

A

Amphotericin B and flucytosine

478
Q

Long term maitenance therapy for crytpococcal meningoencephalitis

A

Fluconazole

479
Q

Tay sachs is caused by beta hexosaminidase A deficiency which results in accululation of the cell membrane glycolipid _______ within lysosomes

A

GM2 ganglioside

480
Q

_______ clinical presentation includes macrocephaly, abnormal startlereflex with acoustic stimuli, and cherry red macula spot

A

Tay sachs

481
Q

Tetrodotoxin (in puffer fish) and saxitoxin (dinoflagellates in “red tide”) bind to Na channels to what effect

A

Inhibit Na influx and prevent action potential conduction

482
Q

Ciguatoxin (in exotic fish and moray eel) and batrachotoxin (in south american frogs) bind to Na channel to what effect

A

Keep it open and cause persitent depolarization

483
Q

Treatment after tetrodotoxin exposure

A

Supportive care and intestinal decontamination with gut labage and charcoal

484
Q

Cytotoxic (ionic) edema begins hours after ischemic injury due to ____ and failure of _______

A

Decreased ATP

ATP dependent ion pumps

485
Q

______ edema follows 24-48 after ischeimc stroke when release of inflammatory mediators disrupts tight jnctions of blood brain barier, allowing proteins and water to enter the inerstitial space

A

Vasogenic

486
Q

A _______ appears as a hyper dense mass on CT and almost always affects the adjacent internal capsule, leading to dysarthria, contralateral hemiparesis, and contralateral hemisensory loss

A

Putaminal hemorrhage

487
Q

The basal ganglia are supplie by the ____ arteries which are deep, small vessel branches off the middle cerebral arteries

A

Lenticulostriate

488
Q

Injury of what nerve can occur due to repetitive pressure/trauma caused by an ill-fitting crutch (crutch palsy) or if an individual sleeps witht he arm over a chair (saturday night palsy)

A

Radial

489
Q

The iliohypogastric nerve arises from L1, emerges from lateral border of the upper psoas major, and passes behing the kidney. It provides motor function to ____

A

Anterolateral abdominal wall muscles

490
Q

Damage to the anterior branch of the _______ nerve during appendectomy causes decreased sensation at the suprapubic region

A

Iliohypogastric

491
Q

In a positive/pathologic jaw jerk reflex, Tapping on the chin with the mouth open will cause what

A

The jaw to briskly close

492
Q

Patients with bilateral _____ lesions will have a positive jaw jerk reflex

A

Upper motor neuron

493
Q

The jaw jerk reflex begins with afferent signals from the muscle spindles of the masseter that are carried along the ______ nerve and the efferent signals travel along the ____ nerve to the muscles of mastication

A

CN V3

CN V3

494
Q

What nerve is injured in tennis elbow

A

Median nerve

495
Q

The median nerve passes between what structurs which allows it to be suseptible to compression

A

Humeral and ulnar heads of the pronator teres muscle

496
Q

How does impaired sensation from compression of the median nerve differ in carpal tunnel syndrome and compression by pronator teres

A

Carpal tunnel syndrome –> impaired sensation to palmar aspects offirst 3 and 1/2 digits
Compression by pronator teres –> impaired senesation to first 3 and 1/2 digits and entire lateral plm and thenar eminence (because also includes palmar branch)

497
Q

In the CNS, serotonergic neurons are primarily found in the _____ nuclei of the brainstem

A

Raphe

498
Q

What medication used in TB treatment is similar to pyridoxine (vit B6) and therefore competes with B6 in the snthesis of multiple neurotransmitters – > defective and products

A

Isonizid

499
Q

Isoniazid increases the urinary excretion of ___ and causes afrank deficiency in it

A

Pyridoxine (vit B6)

500
Q

Trycyclic antidepressants modulate pain transmission by inhibitting ______ in sensory nerves and increasing ______ signaling in the CNS

A

Voltage gated sodium channels

Norepinephrine

501
Q

SNRIs alter central transmission of pain by increasing ______ in the central synapses

A

Norepinephrine

502
Q

What is the term for brief loss of muscle tone precipitated by strong emotion (laughter, excitement)

A

Cataplexy

503
Q

DSM-5 diagnostic criteria of narcolepsy includes low CSF levels of ____

A

Hypocretin-1

504
Q

Narcolepsy with cataplexy is most often caused by the lack of 2 related neuropeptides: hypocretin-1 and hypocretin-2 which are produced in neurons located in _______

A

Lateral hypothalamus

505
Q

The ___ is a component of the basal ganglia that plays an important role in modulation of basal ganglia output. If damaged, it can decrease excitation of the globus pallidus internus –> reducing inhibition of the thalamus

A

Subthalamic nucleus

506
Q

What is the term for a movement disorder that is characterizedby wild,involuntary, large-amplitude, fliging movements invoving the proximal limbs on ones side of the body

A

Hemiballism

507
Q

A lacunar stroke causing damage to the _______ may result in contralateral hemiballism

A

Subthalamic neuclues

508
Q

______ headaches are often recurrent, unilateral, and can be accompaied by ipsilateral autonomic symptoms

A

Cluster

509
Q

thiamine (vit B1) is a cofactor in many enzymes, including _____ which converts pyruvate to acetyl co a

A

Pyurvate dehydrogenase

510
Q

Thiamine (vit B1) isa cofactor for many enzymes including ____ which an an anzyme in the citric acid cycle

A

Alpha ketoglutarate dehydrogenase

511
Q

Thiamine (vit B1) is a cofactor for many enzymes including _____ whch is esential for catabolism of branched chain amino acids

A

Branched-chain alpha ketoacid dehydrogenase

512
Q

Thiamine (vit B1) is a cofactor for many enzymes including _____ which is an enzyme in the pentose phosphate pathway that help convert ribulose 5-P to glycolysis intermediates

A

Transketolase

513
Q

Thiamine deficiency results in decreased ______ utilization which is especialy pronounced in the CNS

A

Glucose

514
Q

Thiamine deficiency can be diagnosed if baseline erythrocyte ______ activity is low but increases after additno of thiamine pyrophosphate

A

Transkelotasee

515
Q

The quadricalent conjugate vaccine for neisseria meningitisis moa

A

Capsular polysaccharide antigens are fused to a diptheroid toxin carrier – > APCs present it to T-cells

516
Q

Serogroup B vaccine for neiserria meningitidis moa

A

Recombinant proteins (instead f the capsular polysaccharides because too close to humn neural cell adhesion molecules –> molecular mimicry)

517
Q

Women in the postpartum period are at particulary high risk of developing what condition which causes fatigable skeletal muscle weakness

A

Mysthenia gravis

518
Q

The most common underlying cause of focal-onset seizures is a _______

A

Focal structural brain abnormality

519
Q

____ is when an initial embryonic disturbance leads to multiple malformations by disrupting th development of adjacent tissues and structures within a particular region

A

Developmental field defect

520
Q

______ referes to complete absence of an organ

A

Agenesis

521
Q

______ refers to multiple anomalies without a known unifying cause that occur together more frequenly than chance alone would predict

A

Association

522
Q

____ are fetal structural anomalies that occur due to extrinsic mechanical forces

A

Deformation

523
Q

______ is a developmental field defect characterized by a spectrum of fetal anomalies due to incomplete division of the forebrain (prosencephalon)

A

Holoprosencephaly

524
Q

What nerve passes posterior to the medial epicondyle of the humerus (cubital tunnel)

A

Ulnar nerve

525
Q

The ulnar nerve innervates the _______ (wrist flexion and adduction) and medial portion of the _______

A

Flexor carpi ulnaris

Medial portion of flexor digitorum profundus

526
Q

The ulnar nerve enters the wrist throught the ______

A

Guyon canal (between hook of hamate and pisiform)

527
Q

The superficial branch of the ulnar nerve provides cutaneous inervation to ______, ____, and _____

A

5th digit
Medial half of 4th digit
Hypothenar eminence

528
Q

Ramelteon MOA

A

Melatonin agonist

529
Q

Neurologic damage associated with ____ dficiency classically includes subacute combined degeneration of the dorsal column, lateral corticospinal tracts, and spinocerebellar tracts

A

Vit B12 (cobalamin)

530
Q

Patients may develop atrphic glossiis, which appears as a smooth, shiny, erythematous tongue following a gastrectomy due to what

A

Vit B12 deficiency

531
Q

Repetitive pronation/supiination of the forearm (ex. Frequent screwdriver use) could injure the radial nerve at what location

A

Supinator muscle

532
Q

What nerve is most frequently injured during axillary lymph node diseection and results in sensory dysfunciton in medial upper arm

A

Intercostobrachial nerve

533
Q

Damage to what nerve results in winging of the scapula

A

Long thoracic

534
Q

What nerve innervates the latissimu dorsi

A

Thoracodorsal

535
Q

Opsoclonus-myoclonus syndrome: nonrhythmic conjugate eye movements and involuntary jerking movements of the trunk and limbs in a young patient should prompt evaluation for _______

A

Neuroblastoma

536
Q

Neuroblastoma arises from _____ cells of the adrenal medula or sympathetic ganglion

A

Neural crest

537
Q

A majority of patients with neuroblastoma have elevated _______ due to the neural crest origin

A

Catecholamine metabolites

538
Q

Biopsy of neuroblastoma mass will reveal _____ and ______

A

Small round blue cells

Homer wright rosettes

539
Q

Tumor tissue of a neuroblastoma is tested for _____ amplification which predicts a poor prognosis

A

N-myc

540
Q

What are the benefits of injecting epinephrine with lidocaine

A

Epinephrine –> vasoconstriction–> decreased local bleeding, prolonged duration of action bc lidocaine stays in site of injection longer, and decreased systemic absorption reducing side effect risks

541
Q

_____ disease can cause cystic degeneration of the putamen as well as other basal ganglia structures

A

Wilsons

542
Q

Schwannomas appear biphasic, microscopically, with highly cellular areas: ______ pattern; intermixed with myxoid regions of low cellularity: _____ pattern

A

Antoni A

Antoni B

543
Q

The Antoni A areas in a schwannoma is composed of _____ cells (eloongated cells with regular oval nuclei) that form palisading patterns interspercing nuclear free zones called ______

A

Spindle

Verocay bodies

544
Q

Schwannomas and melanoma are ___ positive because they are derived from neural crest cells

A

S-100

545
Q

Schwannomas can arise from the peripheral nerves, nerve roots, and cranil nerves except for ____

A

Cranial nerve II (optic nerve)

546
Q

High solubility of anesthetic in the blood (blood/gas partition coefficient) has what effect on time for it to get to the brain

A

More anesthetic must be absorbed by the blood before it can effectively be transfered to other tissues

547
Q

Solubility of an anesthetic in peripheral tissues _______ affects brain saturation

A

Negatively

548
Q

High solubility of anesthetic in the peripheral tissues has what effect on ateriovenous concentration gradient

A

Increases it

549
Q

Mechanism of action of erenumab (migraine treament)

A

Anti-CGRP antibodies

550
Q

Tetrahydrobiopterin (BH4) is a cofactor in the synthesis of _____, ____, and ______

A

Serotonin
Tyrosine
DOPA (tyrosine –> DOPA)

551
Q

Serotonin (5-hydroxytryptamine) is formed through hydroxylation and decarboxylation of the amino acid _____

A

Tryptophan

552
Q

A BH4 deficiency secondary to dihydropteridine reductase deficiency can cause the build up of tryptophan and what other amino acid

A

Phenylalanine

553
Q

Key features of congenital toxoplasmosis infection

A

Chorioretinitis
Hydrocephalus
Diffuse intracranial calcifications

554
Q

Key features of congntial syphilis infection

A

Rhinorrhea
Skeletal anomalies
Desquamating rash (palms/soles)

555
Q

Key features of congenital rubella infection

A

Cataracts
Heart defects (PDA)
Sensrineural hearing loss

556
Q

Key features of congenital cytomegalovirus infection

A

Periventricular calcifications
Microcephaly
Sensorineural hearing loss

557
Q

Key feature of congenital herpes simplex virus infection

A

Vesicular/ulcerative rash

558
Q

What are the TORCH infections

A
Toxoplasmosis
Other infections
Rubella
Cytomegalovirus
Herpes simplez
559
Q

When are TORCH infections contracted

A

In utero due to transplacental transmission

560
Q

What may cause new onset focal neurologic deficits 3-12 daysafter subarachnoid hemorrhage develops

A

Cerebral vasospasms –> delayed cerebral ischemia

561
Q

Subarachnoid hemorrhage is most often caused by rupture of a ______ which occurs frequently in patients with autosomal dominant polycystic diseas

A

Saccular (berry) aneurysm

562
Q

What can be administered to patients to improve outcomes of subarachnoid hemorrhage

A

Nimodipine (selective calcium chanel blocker)

563
Q

How does nimodipine improve outcomes of patients with cerebral vasospasms followign a subarachnoid hemorrhagee

A

Induces cerebral vasodilation and decreases calcium dependent excitotoxicity

564
Q

The sensor limb of the corneal reflex is mediated by CN V1 which enters the orbit through the ______

A

Superior orbital fissure

565
Q

Globe adduction is mediated by the medial rectus muscle which is innervated by the occulomotor nerve (III) which enters the orbit through the ____

A

Superior orbital fissure

566
Q

What nerves enter the orbit via the superior orbital fissure

A
Oculomotor nerve (III)
Opthalamic nerve (V1)
Trochlear nerve (IV)
Abducens nerve (VI)
567
Q

The ___ nerve is a branch of the mandibular nerve (V3) which innervated the lower teeth and is culnerable to injury during dental procedures

A

Inferior alveolar

568
Q

The inferior alveolar nerve gives off the _____ nerve which conveys sensory information from the chin and lower lip

A

Mental

569
Q

A history of gait dysfunction and evidence of myelin/axonal degeneration in the dorsal columns and corticospinal tract are highly suggestive of _____ deficiency

A

Vitamin B12

570
Q

Spinal cord damage seen with vitamin B12 deficiency is called ____________

A

Subacute combined degeneration (combined bc degeneration of both ascending and descending pathways)

571
Q

The brachial plexus originates from the ___- ___ spinal nerve roots and pass between the anterior and middle scalene

A

C5-T1

572
Q

Interscalene nerve block, a technique used for procedures involving shoulder and upper ar, transverses along the interscalene sheath and affects the roots of the ____ nerve (C3-C5)

A

Phrenic nerve

573
Q

Most common primary cerebral neoplasm in adults

A

Glioblastoma

574
Q

Gliobltomas arise from ____

A

Atrocytes

575
Q

What is a butterfly glioma

A

Glioblastoma tha crosses the corpus collosum

576
Q

On gross examination, glioblasomas are soft and poorly defined with area of necrosis and _____

A

Hemorrhage

577
Q

What is the prognosis of glioblastomas

A

Poor, they are highly malignant

578
Q

Levadopa is the immediate precursor to ____

A

Dopamine

579
Q

Dopamine is absent in the ______ of patients with Parkinson disease

A

Nigrostriatum

580
Q

Dopamine itself cannot be administered directly due to its inability to ____

A

Cross the blood brain barrier

581
Q

Levadopa is rapidly metabolized in the peripheral tissues to dopamine and _______

A

3-O-mthyldopa (via catecgol-O-methyltransferase)

582
Q

Levodopa is typically administered with _______, a peripheral DOPA decarboxylase inhibitor

A

Carbidopa

583
Q

Moa: entacapone

A

COMT inhibitor (inhibits peripheral methylation of levodopa)

584
Q

What can be used to treat parkison patients with motor fluctuations who are experiencing end of dose wearing off periods with levodopa/carbidopa therapy

A

COMT inhibitors (entacapone)

585
Q

Inflammation in bacterial meningitis is driven by subcapsular components, partcularyly macromolecules of bacterial cell such as ____ and ___

A

Teichoic acid

Peptidoglycan

586
Q

_____ is the leading cause of bacterial meningitis in adults

A

Strep pnumoniae

587
Q

For patients with strep pneumo meningitis: Pretreatment of ______ reduces levels of inflamator cytokines in the CSF and limits risk of inflammation induced morbidity

A

Dexamethasone

588
Q

Which of the following benefit from pretreatment with dexamethasome and why: strep pneumo, h. Flu, n. Menngitidis

A

Strep pneumo
H. Flu and N. Meningitidis have thinner cell walls (gram negative) so have less peptidoglycan and no teichoic acid and therefore result in less inflammatory cytokine release

589
Q

Creutzfeldt-jacob, fatal familial insomnia, and kuru are all examplse of ____ diseases

A

Prion

590
Q

Prion diseases are progressive neurodegenerative disorders caused by accumulation of _____ within the brain

A

Abnormally folded protein

591
Q

Prion diseases may be transmitted between species how?

A

Ingestion of tainted meat

592
Q

Prion proteins are found in both neuronal and nonneruonal brain cells and normally exist in ______ structure

A

Alpha helical (PrPc)

593
Q

Prion disease occurs after a domain in the prion protein undergoes a conformational change from the alpha helix into ____

A

Beta pleated sheet (PrP^Sc) (scrapie)

594
Q

The beta sheet confirmation of prion proteins are resistant to ____ and form long neurotoxic fibrils which accumulate intracellularly in neurons and form extracellular deposits

A

Proteases

595
Q

On microspcopy of prion diseases, there is a ______ degeneration of gray matter which is characterized by formation of microscopi ____ within the neuronal processes

A

Spongiform

Vacuoles

596
Q

Extracellular prion accumulations (kuru plaques) are frequently present in prion disease and stain positive with ____ and ____ stains

A

Congo red

Periodic acid-Schiff

597
Q

The oculomotor nerve is most susceptible to injury from ipsilateral _______ artery aneurysms

A

Posterior communicating artery

598
Q

Classic manifestation of ______ mass include obstructive hydrocephalus from aqueductal stenosis and dorsal midbrain (Parinaud) syndrome due to direct compression of the pretectal region of the midbrain

A

Pineal gland mass

599
Q

______ syndrome is characterized by limitation of upwrd gaze with a downward gaze preference, bilteral eyelid retraction, and light-near dissociation (pupils react to accomodation but not light

A

Parinaud

600
Q

The most common pineal mass is a _______, a midline tumor thought to arise from embryonic germ cells

A

Germinoma

601
Q

Suprasellar germinomas (less common site for a germinoma) do not lead to Parinaud syndrome, but they are more likely to present with _________

A

Endocrinopathies (central precocious puberty, diabetes insipidus)

602
Q

The ____ nerve innervates the quadricepsmuscles and provides sensation for the arch of the foot, shin, and anteromedial thigh

A

Femoral

603
Q

The optimal site for a femoral nerve block is right below the _____ at the lateral border of the femoral artery

A

Inguinal ligament

604
Q

What nerve that passes through the cavernous sinus next to the internal carotid arter is the most likely structure to be damaged by an expanding aneurysm of the internal carotid

A

Abducens (VI)

605
Q

Esotropia

A

Inward eye deviation

606
Q

Occlusion of the _______ artery would affect sensory and motor function of the contralateral leg and foot while predominntly sparing contralateral arm/face

A

Anterior cerebral artery

607
Q

Patients with bilateral ______ atery occlusions can develop significant behavioral symptoms and urinary incontinence if the frontal micturition center (medial frontal lobe/cingulate girus) is affected

A

Anterior Cerebral artery

608
Q
Oclussion of the anterior cerebral artery would most likely impair what movements: 
Climbing stairs
Gripping
Speaking
Swallowing food
Whistling
A

Climbing stairs

609
Q

The etiology of narcolepsy is believed to be due to low levels of the stimulatory neurotransmitter ______ which isinvolved in maintaining wakefulness and supressing REM sleep-related phenomena

A

Orexin (hypocretin)

610
Q

Modafinil MOA

A

Nonamphetamine stumulant, may enhance dopaminergic signaling (first line agent for narcolepsy bc effective, well tolerated and misuse is rare)

611
Q

Bells palsy is idiopathic paresis of ______ nerve

A

Facial (CN VII)

612
Q

What nerve sends parasympathetic innervation to the lacrimal, submandibular, and sublingual salivary glands

A

Facial (VII)

613
Q

What nerve sends afferent fibers for taste for anterior 2/3 of tongue

A

Facial

614
Q

What nerve sends somatic afferents from the pina and external auditory canal

A

Facial

615
Q

Specific findigs of bells palsy tipically include impaired eye closure, eyebrow sagging, inability to smile and frown on affected side, disappearance of the _____ fold and the mouth being drawn to the _____ side

A

Nasolabial

Non affected

616
Q

Patients with bells palsy may experience ___ tearing, hyper____, and loss of taste sensation over the ______ of the tongue

A

Decreased
Acusis
Anterior 2/3

617
Q

Gross examination of hemangiomas reveals a “mulberry-like” appearance due to their purple vascular clusters. Histologically they are composed of abnormal, dilatd blood vessels with a thin adventitia lacking ______ and ______

A

Elastic fibers

Smooth muscel

618
Q

Cavernous hemanigiomas’ reduced structural suppor givesthem a tendency to leak, causing recurrent ______

A

Hemorrhage

619
Q

_____ hematoma has a clinical manifestation of lucid interval followed by loss of consciousness

A

Epidural

620
Q

_____ hematoma has a clinical manifestation of coma at onset and chronic gradual onset of headache and confusion

A

Subdural

621
Q

What vessel is tpically involved in epidural hematoma

A

Middle meningeal artery

622
Q

What vessel is typically involved in subdural hematoma

A

Bridging cortical veins

623
Q

How is a subarachnoid hemorrahage visualized on CT? Blood in the _____

A

Basal cisterns

624
Q

Epidural is accumulation of blood between the ____ and_____

A

Skull bone

Dura mater

625
Q

Most cases of epidural hematoma are due to fracture of the ______

A

Pterion region of the skull

626
Q

An ipsilateral dilated pupil can occur during an epidural hematoma due to ___ herniation and _____ nerve compression

A

Uncal

Oculomotor

627
Q

The diagnoses of epidural hematoma can be confirmed by ______ showing a hyperdense, biconvex (lens-shaped) mass between the brain and skull

A

Non contrast CT

628
Q

_____ are extracellular deposits often found in the medial temporal lobe and are composed of a central amyloid beta core surrounded by dystrophic neurites

A

Neuritic (senile) plaques

629
Q

______ are found int he neuronal cytoplasm and consist of aggregates of hyperphosphorylated tau protein, which normally mediates micrtubule stabilization

A

Neurofibrillary tangles

630
Q

Symptoms of normal pressure hydrocephalus are progressive ad occur due to disruption of periventricular _____ by the expanding ventricles

A

White matter tracts

631
Q

Treatment for normal pressure hydrocephalus

A

Large volume CSF removal and longterm treatment frequently involves placement of a ventriculoperitoneal shunt

632
Q

Psuedopalisading necrosis is an area of necrosis surounded by columns of ______

A

Tumor cells

633
Q

Pseudopalisading necrosis with vascular proliferation (capillaries at the periphery) are characteristic histologic finsings of ______

A

Glioblastoma multiforme

634
Q

Glioblastoma multiforme is usually located within the cerebral hemispheres and often presents with _______ that worsens with bending over and ____, ____, and /or _____

A

New onset headache
Nausea/vomiting
Focal neurological defects
Seizures

635
Q

___ is the most common cause of spontaneous lobar hemorrhage, particularly in adults over age 60

A

Amyloid angiopathy

636
Q

Amyloid angiopathy is a consequence of ____ deposition in the walls of small- to medium- sized cerebral arteries resulting in vessel wall weakening and predisposition to rupture

A

Beta amyloid

637
Q

Dopamine agonists have a chemical structure similar to dopamine and directly stimulate the dopamine receptor. Do they need to be metabolized to be active?

A

No

638
Q

What are the two classes of dopamine agonists

A
Ergot compounds (derive from ergot fungi; bromocriptine)
Nonergot compounds (pramipexole, ropinirole)
639
Q

MOA bromocriptine

A

Dopamine agonist (ergot compound)

640
Q

MOA pramipexole

A

Dopamine agonist (nonergot compound)

641
Q

MOA ropinirole

A

Dopamine agonist (nonergot compound)

642
Q

The tetanus toxin blocksi nhibitory interneurons at what location in the body?

A

Anterior horn cells

643
Q

Cerebral spinal fluid is formed by 4 ___ found in each of the ventricles

A

Choroid plexuses

644
Q

CSF flows from the lateral ventricles to the third ventricle via the ______

A

Interventricular foramina of monro

645
Q

CSF travels from the 3rd ventricle to the 4th ventricle via the _____

A

Cerebral aqueduct (of Sylvius)

646
Q

CSF exits the 4th ventricle and enters the subaracnoid space via one of the 3 foramina: the 2 lateral foramina of ________ and the single midline foramen of ______

A

Lushka

Magendie

647
Q

CSF is returned to venous circulation from the subarachnoid space via ______

A

Arachnoid villi (granulations)

648
Q

_________ presents with elevated ICP and classically occurs in young women who are overweight. The etiology is not well known but it is thought to be related to cerebral venous outflow abnormalities due to elevated intracranial pressure

A

Pseudotumor cerebri

649
Q

Malignant hyperthermia is oftern due to abnormal ____ in skeletal muscle

A

Ryanodine receptors

650
Q

______ is used to treat malignant hypertension because it directly inhibits intracellular calcium release fom the abnormal ryanodine receptor

A

Dantrolene

651
Q

Selegiline MOA

A

Inhibitor of MAO type B

652
Q

Clinical use of Selegiline

A

Delays progression of Parkinson disease (prevents damage to dopamanergic neurons)

653
Q

What is the likely diagnosis: 16 yr old boy with chronic loss of upper extremity pain and temp sensation, upper extremity weakness and hyporeflexia, lower extremity weakness and hyperreflexia, and kyphoscoliosis

A

Syringomyelia

654
Q

Name the hereditary disease that causes degeneration of spinocerebellar tracts, posterior colums and dorsal root ganglia

A

Friereich ataxia

655
Q

What is the most common cause of death in friedreich ataxia

A

Hypertrophic cardiomyopathy

656
Q

What skeletal anormalities are seen in friedrich ataxia

A
Kyphoscoliosis
Pes cavus (high arches)
657
Q

What inherited disease may present with behvioral abnormalities (mood changes, withdrawl), cognitive impairment, and chorea (jerky, fidgety, involuntary movements)

A

Huntington disease

658
Q

What neurons in the caudte nuclei (striatum) are especialy vulnerable and atrophy early in the course of Huntington disease

A

Inhibitory GABAnergic neurons

659
Q

Expanding space occupying lesions such as hemorrhage or hematoma can manifest with Cushing triad which is what

A

Hypertension, bradycardia, irregular respirations

660
Q

Lesions in the temporal lobe tend to cause what form of herniation

A

Transtentorial herniation of the uncus

661
Q

Transtentorial herniation of the uncus can compress the ipsilateral _____ nerve as it exits the midbrain at the same level

A

Oculomotor nerve (CN III)

662
Q

Compression of CNIII due t trnastentorial herniation of the uncus can lead to what pupil finding

A

Dilated pupil

663
Q

The left temporal hemiretina joins the right nasal hemiretina and travels via the left optic tract to the left _______ in the thalamus

A

Lateral geniculate body

664
Q

Visual signals leave the lateral geniculate body and travel via optic radiations to the ipsilateral ______ for visual processing

A

Primary visual cortex

665
Q

Herpes zoster opthalmicus is caused by viral reactivation involving what nerve

A

Trigeminal nucleus –> opthlmic branch of trigeminal nerve

666
Q

How can herpes zoster affecting the opthalmic branch of the trigeminal nerve lead to blindness

A

CN V1 conveys sensory information from the cornea, if theres a lesion it can lead to blindness due to acute keratitis

667
Q

What inheritable disease is characterized by initial degeneration of the prefrontal cortex that eventually progresses to include the anterior temporal cortex

A

Frontotemporal dementia

668
Q

What subtype of demetia has these characteristic findings:
Early insidious short term memory loss
Language deficits and spatial disorientation
Later personality changes

A

Alzheimer disease

669
Q

Wha subtype of dementia presents with:
Stepwise decline
Early executive dysfunction
Cerebral infarction and/or deep white matter changes on neuroimaging

A

Vascular dementia

670
Q

What subtype of dementia may present with the following:
Early personality changes
Apathy, disinhibition and compulsive behavior
Frontotemporal atropthy on neuroimaging

A

Frontotemporal dementia

671
Q

What subtype of dementia may present with the following:
Visual hallucinations
Spontaneous parkinsonism
Fluctuating cognition
Rapid eye movement sleep behavior disorder

A

Dementia with lewy bodies

672
Q

What subtyme of dementia may present with the following
Ataxia early indisease
Urinary incontinence
Dilated ventricles on neuroimaging

A

Normal-presure hydrocephalus

673
Q

What subtype of dementia may present with the following:
Behavioral changes
Rapid progression
Myclonus and/or seizures

A

Prion disease

674
Q

What area of the brain is responsible for all communicative motor planning

A

Brocas

675
Q

Damage to what part of the brain results in inability to understand spoken language or follow commands (non intact speech comprehension)

A

Wernickes

676
Q

Brocas area is in the caudal part of the inferior ____ gyrus of the dominant hemisphere (which is usually what side?)

A

Frontal

Left

677
Q

Vecuronium mechanism of action

A

Nondepolarizing agent, competitive antagonist of nicotinic acetylcholine receptor

678
Q

Why do patients with myasthenia gravis have increased sensitivity to vecuronium and other nondepolarizing neuroblocking agents

A

They have low number of functioning receptors

679
Q

How do depolarizing neuromuscular blocking agents act differently in patients with myathenia gravis

A

Because they have fewer funcitoning receptors, they are more resistant to these agents, larger doses are required to induce muscle relaxation

680
Q

Parianal anestesia with loss of anocutaneos reflex indicates involvement of what nerve roots

A

S2-S4

681
Q

Conus medullaris syndrome involves what spinal region

A

L1-L2

682
Q

Cauda equina syndrome involves what spinal region

A

Below L2

683
Q

Conus medullaris syndrome typically causes ____ (bilateral/unilateral) extremity weakness with ____ motor neuron signs

A

Bilateral

Upper

684
Q

Cauda equina syndrome tends to cause ______(symetric/assymetric) lower extremity weakness with _____ motor neuron signs

A

Assymetric

Lower

685
Q

What is a funciton of the frontal lobe and may be tested by asking a patient to describe the similarities between two objects

A

Abstraction

686
Q

A patient with recurrent headaches and seiures with multiple flow voids on MRI is consitent with what diagnosis

A

Cerebral arteriovenous malformations

687
Q

What are vascular malformations inwhich blood courses directly from arteries to veins without passing through an intervening capillary bed allowing turbulent flow which can lead to aneurysm development, bleeding, and damage to the surrounding brain

A

Arteriovenous malformations

688
Q

Arteriovenous malformations can appear as what on angiography and what on MRI

A

Bag of worms

Dark flow voids(indicative of swift blood flow)

689
Q

What travels through the cribiform plate

A

CNI olfactory bundles

690
Q

What traves through the optic canal

A

CN II
Opthalmic artery
Central retinal vein

691
Q

What travels through the superior orbital fissure

A

CN III, IV, V1, VI
Opthlmic vein
Sympathetic fibers

692
Q

What travels through the foramen rotundum

A

CN V2 (maxilary)

693
Q

What travels through the foramen ovale

A

CNV3 (mandibular)

694
Q

What travels through the foramen spinosum

A

Middle meningeal artery and vein

695
Q

What travels through the internal acoustic meatus

A

CN VII, VIII

696
Q

What travels through the jugular foramen

A

CN IX, X, XI

Jugular vein

697
Q

What travels through the foramen magnum

A

Spinal roots of CNXI
Brain stem
Vertebral arteries

698
Q

What travels throught he hypoglossal canal

A

CN XII

699
Q

What nerve innervates hte muscles of mastication

A

CNV3

700
Q

What three muscles close the jaw

A

Masseter
Medial pterygoid
Temporalis

701
Q

What muscle opens the jaw

A

Lateral pterygoid

702
Q

Unilateral injury of CNV leads to deviation of the jaw to what side

A

Ipsilateral side (due to unopposed action of the contralateral pterygoid)

703
Q

What somatic nerve function does the glossopharyngeal nerve have

A

Styolopharyngeus muscle (only): elevates larynx during swallowing

704
Q

The sciatic nerve branches into the _____ and ___ nerve just proximal to the popliteal fossa

A
Common fibular (peroneal) nerve
Tibial nerve
705
Q

After coursing around the ______ the fibular nerve divdes into the deep and superficial branches

A

Neck of fibula

706
Q

The ____ branch of the fibular nerve innervates the anterior compartment muscles of the leg (foot and toe dorsiflexion)and provides senstion to the webspace between the first and second toes

A

Deep

707
Q

The ___ branch of the fibular nerve innervates the lateral compatment muscles (foot eversion) and providessensation to the dorsum of the foot and lateral shin

A

Superficial

708
Q

The ____ nerve is frequently injured by trauma due to its superficial location at the neck of the fibula

A

Common fibular

709
Q

Temporal lobe epilepsy is the most common type of _____ epilepsy which occur when partial seizures originate from one area of the brain and are usualy due to an underlying structural disorder which serves as an epileptogenic focus

A

Localiztion-related

710
Q

Temporal lobe epilepsy is most commonly due to _______ which is usually visible as ______ on MRI

A

Hippocampal sclerosis

Hippocampal atrophy

711
Q

Characteristic histopathological findings in hippocampal sclerosis includes atrophy of the hippocampal neuons with marked reactive gliosis: proliferation of ____ in response to injury

A

Astrocytes

712
Q

The rabies virus contains a bullet shapd envelope with knob like glycoproteins that allow it to attach to the ________ at the neuromuscular junction

A

Nicotinic acetylcholine receptor

713
Q

A patient with sudden onset explosive headache, brief loss of conscioussness and signs of menigeal irritation most likely has what type of hemmorage

A

Subarachnoid hemorrhage

714
Q

Subarachnoid hemorrhage usually results from the spontaneous rupture of ____-

A

Saccular (berry) aneurysm

715
Q

In subarachnoid hemorrhage, blood empties into the subarachnoid space and pools in _____ and ______

A

Cerebral sulci

Basal cisterns

716
Q

_____ is a transmembrane glycoprotein found in the presynaptic vesicles of neurons, neuroectodermal and neuroendocrine cells

A

Synaptophysin

717
Q

Immunoreactivity of a CNS tumor for synaptophysin indicates a ____ orgin

A

Neuronal

718
Q

Nigrostriatal degeneration in Parkinson disease results in excessive excitation fo the _________ by the subthalamic nucleus, which in turn causes excessive inhibition of the thalamus

A

Globus pallidus internus

719
Q

Patients with medically intactractable symptoms of parkinson disease may benefit from high frequency deep brain stimulation to the globus pallidus internus or. _____

A

Subthalamic nucleus

720
Q

____ is a rare autosomal dominant condition characterized by the presence of capillary hemangioblastomas in the retina and or cerebellum as well as congenital cysts and or neoplasms in the kidney, liver, and pancreas

A

Von hippel lindau disease

721
Q

Microscopically, _____ are well differentiated neoplasms comprised of spindle cells with hair-like glial processes that are associated with micrcysts. These cells are mixed with Rosenthal fibers and granular eosinophilic bodies

A

Pilocytic astrocytomas

722
Q

A cystic tumor in the _____ of a child is most likely a pilocytic astrocytoma

A

Cerebellum

723
Q

Interupting cortical input has what effect on bladder activity

A

–> bladder hyperactivity (urge incontinence)

724
Q

Loss of the pontine micturition center has what effect on urination

A

–> neurogeni bladder

PMC coordinates detrusor contraction and sponcter relaxation

725
Q

Lower spinal cord lessions in the sacral spinal cord such as cauda equina syndrome has what effect on urination

A

–> bladder underactivity (overflow incontinence: unable to completely empty bladder –> overflow which leaks out unexpectedly)

726
Q

The pelvic floor and urinary sphincter muscles are innervated by what nerve roots

A

S2-S4

727
Q

Neuromodulation directed toward S2-S4 nerve roots can improve continence by improving pelvic floor muscle strentgth andcontraction of the external urethral sphincter, it may also impact the ________ refex

A

Bladder stretch-contraction

728
Q

Propofol is a highly ____ anesthetic drug used fo both induction of maintenanceof general anestesia as well as procedural sedation. Onset approximtely 30 sec and duration typically <10 min

A

Lipophilic

729
Q

Following bolus infusion, propofol is rapidly cleared from the plasma and preferentially distributed to organs _______

A

Receiving high blood flow (brain)

730
Q

Because the site of action for propofol is the brain, _____ acounts for the rapid termination of the drug

A

Redistributionn

731
Q

______ is an inflammatory condition that affects the walls of medium sized and large arteries with granulomas

A

Temporal arteritis (aka giant cell vasculitis)

732
Q

On light microscopic exam of temporal arteritis, granulomas are seen in the ____ of the arteries consisting of mononuclear infiltrates and multinucleated giant cells

A

Media

733
Q

Commonly reported symptoms of temporal arteritis include:

A

Headache (focal pain over temple)
Craniofacial pain syndromes
Polymyalgia rheumatica
Sudden vision loss (may be transient or permanent)

734
Q

What symptom commonly occurs in temporal arteritis and is characterized by neck, torso, shoulder, and pelvic girdle pain and morning stiffness. Fever, fatigue, and weight loss may also occur

A

Polymyalgia rheumatica

735
Q

An indirect inguinal hernia is protrusion of abdominal contets through the abdominal wall via the _______

A

Deep/internal inguinal ring and inguinal canal

736
Q

A direct inguinal herni is protrusion othe abdominal contents through the abdominal wall via the _______

A

Superficial inguinal ring

737
Q

Define allodynia

A

Pain caused by normally nonpainful stimuli

738
Q

The ____ nerve enters the inguinal canal anterior to the internal ring and follows the spermatic cord to the superficial ring

A

Ilioinguinal nerve

739
Q

The ilioinguinal nerve gives off sensory branches to the anterior scrotum/labia majora, base of penis/mons pubis, and _____

A

Medial thigh

740
Q

What is the Uhthoff phenomenon, seen in multiple sclerosis

A

Symptoms worsening with increased body temperature

741
Q

What gene increases the risk of having multiple sclerosis

A

HLA-DRB1

742
Q

What is Lhermitte sign, seen in multiple sclerosis

A

Electrical sensations down the back/limbs with neck flexion

743
Q

In multiple sclerosis, demyelinating plaques are commonly seen as hyperintense lesions on _____ MRI

A

T2-weighted

744
Q

In diabetic CNIII mononeuropathy, why is pupillary size and reactivity often normal while the extraocular muscles supplied by CNIII are usually affected causing a down and out positioning

A

It is due to ischemia predominately involving the core of CN III (where somatic nerve fibers travel) while sparing the outer regions (where autonomic component is located)

745
Q

Recurrent focal impaired awareness seizures that are preceded by a distinctive aura are characteristic of ____ epilepsy

A

Mesial temporal lobe

746
Q

Patients with arteriovenous malformations may have seizures which may be due to ____ accumulation, which is a cortical irritant, from microbleeds

A

Hemosiderin

747
Q

What cause of headaches can also cause ipsilateral autonomic symptoms due to parasympathetic hyperactivity such as nasal congestion, lacrimation, ptosis, miosis and conjunctival injection

A

Cluster headaches

748
Q

____ are transient episodes of focal neurologic impariment that occur due to local brain ischemia, tissue infarction does not occur, and brain imaging is normal

A

Transient ischemic attacks

749
Q

The trochlear nerve innervates_____ muscle which causes the eye to intort and depress when adducted

A

Superior oblique

750
Q

Patients with trochlear nerve palsy typically present with ____ which is most noticeable when the afected eye looks down and toward the nose (close up reading, going down stairs)

A

Vertical diplopia

751
Q

People may compensat for ____ nerve palsy by tucking their chin and tilting their head away from the affected side

A

Trochlear

752
Q

What autoimmune disorder is characterized by fatigable muscle weakness that most commonly affects the eyes, blulbar, facial, and proximal muscles

A

Myasthenia gravis

753
Q

HIV associated dementia is due to a change of viral tropism from replicating in CD4 cells to microglil and ______ which alows the virus to penetrate deeper in the brain parenchyma

A

Macrophage

754
Q

uncal herniation is herniation of the medial temporal lobe (uncus) through the _____

A

Tentorial notch

755
Q

In uncal herniation, compression of the _____ leads to an ipsilateral fixed and dilated pupil

A

Ipsilateral occulomtor nerve

756
Q

In uncal herniation, compression of ____ leads to contralateral homonymous hemianopsia with macular sparing

A

Isilateral posterior cerebral artery

757
Q

In uncal herniation compression of the ______ of the midbrain against the tentorium may occur, damaging the descending corticospinal tracts and causing contralateral hemiparesis

A

Ipsilateral cerebral peduncle

758
Q

______ parasomnias such as sleepwalking and sleep terrors occur during deep, slow wave sleep

A

Non-REM (NREM)

759
Q

Most dreams occur during ____ sleep

A

REM

760
Q

_____ waves are characteristic of deep, slow wave sleep (stage N3)

A

Delta (frequency up to 3.99 Hz)

761
Q

Alpha and beta waves are characteristic of _______ and _____ sleep

A

Wakefulness and REM sleep

762
Q

____ complexes and sleep _____ are characteristic of stage N2 (light, stable sleep)

A

K

Spindles

763
Q

What stage makes up the largest amount of sleep

A

Non REM stage 2 (N2)

764
Q

What stage of sleep is prominent in the 1st half of sleep and is when sleep walking and night terrors occur

A

Non REM stage 3 (N3)

765
Q

What stage of sleep is prominent in the 2nd half of night and is when nightmare disorder and muscle atonia occurs

A

REM

766
Q

REM’s EEG resembles wakefulness with ocassional _____ waves

A

Sawtooth

767
Q

Diazepam MOA

A

Long acting benzo

768
Q

Diazepam, a long acting benzo can be used in the following: axiolytic, sedative-hypnotic, anticonvulsant, and ___-

A

Muscle relaxant (can stop spasticity caused by upper motor neuron disorders and tetanus)

769
Q

As a class, all benzodiazepines should be excludedfrom use in conjunction with alcohol, babituates, neuroleptics, or ________

A

1st generation antihistamines

770
Q

Chlorpheniramine MOA

A

First generation antihistamine (blocks both central and peripheral H1 receptors)

771
Q

____ is a heterogeneous condition characterized by permanent, nonprogressive motor dysfunction caused by damage to the developing brain

A

Cerebral palsy

772
Q

Spastic cerebral palsy may be caused by white matter necrosis which leads to loss of ________ control from the upper motor neurons

A

Descending inhibitory

773
Q

GABA A receptor mediates a _____ response than GABA B receptors bc it is what type of receptor

A

Faster

Ion gated chloride channel

774
Q

GABA B receptor mediates a _____ response than GABA A becaues it is mediated by _________

A

Slower

G protein coupled receptor that opens pottasium channels

775
Q

Baclofen MOA

A

Agonist of GABA B receptors (can be used to treat spasticity)

776
Q

Medications used to enhance the activity of what neurotransmitter can improve spasticity in cerebral palsy

A

GABA

777
Q

A ____ tremor is also referred to as familial treor as it often follows autosomal dominant inheritance

A

Essential

778
Q

What is the first line treatment for essential tremor

A

Propranolol

779
Q

MOA propranolol

A

Nonspecific beta adrenergic antagonist

780
Q

Lidocaine MOA

A

Blocks sodium channels in neuronal cell membrane

781
Q

Local anestetics ahve a greater effect on ___, _____ nerves, so they preferentially inhibit neurons that carry pain and temp sensation

A

Small myelinated nerve

782
Q

Local anesthetics are weak ____ that exist in charged and uncharged forms

A

Bases

783
Q

Why is a higher dose of local anesthetic required to achieve adequate anesthsia in infected tissue

A
Anesthetic crosses the cell membrane in uncharged form
acidic tissues (such as infected tissues) are more acidic and result in more of the anesthetic existing in the charged form which results in less molecules able to penetrate the cells to block the sodium ion channels
784
Q

Histopathologicfindings of a patients brain with HIV associated dementia includes microglial cells and macrophages clustered around small areas of necrosis (______) and fused together forming____

A

Microglial nodules

Multinucleated giant cells

785
Q

Meningiomas are benign or malignant?

A

Benign

786
Q

Meningiomas typically afect adults and tend to arise near ____

A

Dural reflection

787
Q

Parasagittal lesions compressing the medial portion of the primary somatosensory cortex in the parietal lobe can result in _________ loss with _______ hemineglect if there is also damage to the parietal association cortex (non dominant hemisphere)

A

Contralateral lower limb sensory

Contralateral

788
Q

The thalamic ____ nucleus receives input from spinothalamic tract and dorsal comuln

A

Ventral posterior lateral

789
Q

The thalamic _________ nucleus receives input from the trigeminal pathway

A

Ventral posterior medial

790
Q

The thalamic ventral posterior lateral nucleus and ventral posterior medial nucleus sent ______ projections to the cortex via thalamical fibers

A

Somatosensory

791
Q

Lacunar infarcts result from occlusion of small penetrating arteries that supply deep brin structures (ex. _______) most comonly in the setting of chronic uncontrolled hypertension or diabetes mellitus

A

Lenticulostriate arteries

792
Q

________ , beleived to be one of the primary causes of lacunar infarcts, is characterized by hyaline thickening of the vascular wal, collaggenous sclerosis, and accumulation of mural foamy macrophages

A

Lipohylanosis

793
Q

______, beleived to be a primary cause of lacunar infarcts, result from the atherosclerotic accumulation of lipid-laden macropahges within the intimal layer of a penetrating artery near its origin off the parent vessel

A

Microatheromas

794
Q

CN _____ is pure motor nerve that innervates the sternocleidomastoid and _____

A

XI (spinal acessory nerve)

Trapezius

795
Q

CNXI follows a superficial course through the ___ triangle of the neck and is vulnerable to penetrating trauma and iatrogenic injury (cervical lymphnoid node dissection)

A

Posterior

796
Q

Symptoms of what muscle weakness include drooping of the shoulder, impaired abduction of the above 100 degrees, and lateral displacement of the scapula

A

Trapezius

797
Q

The most common finding in PCA territory infarction is _______ often with macular sparing due to colateral circulation from the middle cerebral artery

A

Contralteral hemianopia

798
Q

The posterior cerebral artery branches off the basilar artery and supplies cranial nerves ___ and _____ and other structures in the midbrain

A

III

IV

799
Q

Fracture of the pterion risks lacerating the _____ artery causing an epidural hematoma

A

Middle meningeal

800
Q

The middle meningeal artery is a branch of the ____ artery (one of the terminal branches of the external carotid artery) which enters the skull at the foramen spinosum and suppies the dura mater and periosteum

A

Maxillary

801
Q

The middle meningeal artery enters the skull through the ____

A

Foramen spinosum

802
Q

Fluent aphasia, characterized by speech that is fluent, well articulated, and melodic but meaningess, is often produced bylesion in the _____ area of the brain

A

Werkicke

803
Q

What artery supplies wernickes area

A

Middle cerebral artery (inferior terminal)

804
Q

“Wernkicke-____ salad”

A

Word

805
Q

Wernickes area is located in the _____ cortex within the posterior portion of the superior temporal gyrus in the dominant temporal lobe

A

Auditory association

806
Q

Motor function of obturator nerve

A

Adduction of the thigh

807
Q

Obturator nerve arises from the lumbar plexus and carries fibers from the _____ spinal segments

A

L2-L4

808
Q

What nerve passes throught the obturator canal

A

Obturator nerve

809
Q

The anterior division of the obturator nerve gives off a terminal cutaneous branch that provides sensation over the ________

A

Distal medial thigh

810
Q

Nightmares occur during REM sleep andcan be differntiated from sleep terrors, a non REM parasomnia characterized by incomplete ____ and lack of _____ of dream content

A

Arousal

Recall

811
Q

______ typically occurs 2-8 weeks after exposure to high risk drugs and patients tyically develop fever, generalized lymphadenopathy, facial edema, diffuse skin rash, eosinophilia, and internal organ dysfunction

A

Drug reaction with eosinophilia and systemic symptoms (DRESS)

812
Q

What nerve supplies the stapedius muscle to reuce volume by dampening ossicle movement in the middle ear

A

Facial nerve (CN VII)

813
Q

The facial nerve provides taste to the anerior two thirds of the tongue via the ______ nerve

A

Chorda tympani

814
Q

Facial nerve palsy results in loss of corneal reflex due to denervation of the _____ muscle

A

Orbiculais oculi

815
Q

A non contrast CT of a subaracchnoid hemorrhage will show what

A

Hypersensiy within the cisterns/sulci

816
Q

____ aneurysms are the most common cause of subarachnoid hemorrhages and are assocaited with ehlers danlos syndrome and autosomal dominant polycystic kidney disease

A

Berry (sacular)

817
Q

In subarachnoid hemorrhage, blood accumlates between the ___ and ____

A

Pia

Arachnoid

818
Q

What type of CT is diagnostic of subarachnoid hemorrhage

A

CT without contrast

819
Q

What will a lumbar puncture reveal with a subarachnoid hemorrhage

A

Gross blood or xanthochromia (yellow discoloration of spinal fluid)

820
Q

Histopathological findings of neurons with shrunken, basophilic nuclei and intensely eoinophilic cytoplasm (red neurons) are indicative of _______

A

Irreversible neuronal damage

821
Q

What is seen on light microscopy of a cryptococcus neoformans infected CSF sample stained with india ink

A

Round or oval budding yeast

822
Q

C4 can be testd with what movement

A

Shoulder/scapular elevation

823
Q

C5 can be tested with what movement

A

Shoulder abduction

824
Q

C5 and C6 can be tested with what movement

A

Elbow flexion, wrist extension

825
Q

C7 can be tested with what movement

A

Elbow extension, finger extension

826
Q

C8 can be tested with what movement

A

Wrist flexion, finger flexion

827
Q

T1 can be tested with what movement

A

Finger abduction

828
Q

What does the biceps and brachioradialis refelxes test

A

C5, C6

829
Q

What nerve roots does the triceps reflex test

A

C7, c8

830
Q

Phase 2 block durring succinylcholine adminatration is similar to a ______ blockade as the nicotinic acetylcholine receptors become gradually desensitized to the effects of succinycholine

A

Non depolarizing

831
Q

How does succinylchoine administration lead to hyperkalemia

A

It acts on nicotinic acetylcholine receptors which are non selective cation channels and alow sodium influx as well as potassium release

832
Q

Why are patients with crush or burn injuries, denerving injuries or diseases, and myopathies at higher risk of hyperkalemia in succinylcholine administration

A

These pathologic states cause up regulation of muscle nicotinic acetylcholine receptors –> large amounts of potassium released

833
Q

What is myotonia

A

Abnormally slow relaxation of the muscles

834
Q

Myotonic dystrophy is an inherited autosomal dominant trait that occurs because of an abnormal trinucleotide repeat expansion of _____

A

CTG

835
Q

The trinucleotide expansion of CTG in myotonic dystrophy codes for what gene

A

Myotonia-protein kinase

836
Q

What are 3 common features seen in myotonic distrophy besides myotonia

A

Cataracts
Frontal balding
Gonadal atrophy

837
Q

Friedreich ataxia is an autosomal recessive disorder caused by a mutation in the frataxin (FXN) gene which codes for an essential mitochondrial protein involved in assembly of _____

A

Iron sulfur enzymes

838
Q

In Friedrich ataxia, a trinucleotide repeat of what of ____ on the mutated FXN gene

A

GAA

839
Q

In Friedreich ataxia, trinucleotide repeats of GAA lead to ______ of FXN

A

Decreased expression

840
Q

Friedreich ataxia has decreased FXN expression which leads to decreased mitochondrial _____ production and increased _______, resulting in degeneration of neural tracts and peripheral nerves

A

Energy

Oxidative stress

841
Q

Psammoma bodies are present in what types of tumors (4)

A

Meningioma
Papillary thyroid carcinoma
Meothelioma
Papillary serous carcinoma of the ovary and endometrium

842
Q

_____ are well circumscribed, round masses attached to the dura and are commonly found at the falcine, parasagittal, or lateral convezity regions of the brain

A

Meningiomas

843
Q

Median nerve injury can lead to pain and numbness in the first 3 digits and lateral half of the third digit, along with weakness of thumb ___ and ____

A

Flexion and opposition

844
Q

Changes seen in the neuronal body after an axon is severed are called ______

A

Axonal reaction

845
Q

What happens to the nucleus in axonal reaction

A

Nucleus is displaced to the periphery

846
Q

The changes in the body of a neuron after the axon has been severed are called axonal reaction, this process reflect an increased ________ that facilitates axonrepair

A

Protein synthesis

847
Q

What are telangiectasias

A

Abnormal dilations of capillary vessels

848
Q

The risk of cancer in patients with ataxia-telaniectasia is increased significantly due to inefficient ____

A

DNA repair

849
Q

Manifestations of _________ , an autosomal recessive disorder, manifests as cerebellar ataxia, oculocutaneous telangiectasia, repeated sinopulmonary infections, and an increased incidence of malignancy

A

Ataxia-telangiectasia

850
Q

Ataxia-telangiectasia is characterized by DNA hypersensitivity to ______

A

Ionizing radiation

851
Q

In __________, DNA is hypersensitive to UV radiation causing premature skin aging and increased risk of skin cancer (melanoma and squamous cell carcinoma)

A

Zeroderma pigmentosum

852
Q

______ anemia is caused by hypersensitivity of DNA to crosslinking agents

A

Fanconi

853
Q

____ syndrome is characterized by generlized chromosomal instability. Increased susceptibility to neoplasms is present

A

Bloom

854
Q

hereditary nonpolyposis colorectal cancer occurs due to defect in ________ enzymes. It leads to increased susceptibility to colon cancer

A

DNA mismatch-repair

855
Q

What is internuclear opthalmoplegia

A

Impaired adduction on the left eye with riht lateral gaze

856
Q

What is optic neuritis

A

Transient blurred vision and eye pain with movement

857
Q

What is saltatory conduction

A

Nerve impulses jumping between 2 adjacent nodes in myelinated axons

858
Q

Why do some of the symptoms and signs of MS resolve to a varible extent

A

Overtime, sodium channels evenually redistribute across the naked axon

859
Q

Sciatic nerve roots

A

L4-L5

860
Q

What nerve is suseptible to injury during hip fracture or arthroplasty because of its proximity to the hip joint

A

Sciatic

861
Q

The sciatic nerve motor function

A

Knee flexion

862
Q

Sciatic nerve divides into what two nerves

A
Common fibular (peroneal)
Tibial
863
Q

What nerve controls plantar flexion and inversion and carries sensory from the plantar surface of the foot

A

Tibial

864
Q

What nerve is tested in the ankle (achilles) reflex

A

Tibial

865
Q

What nerve controls dorsiflexion and eversion of the foot and sensory to the lateral calf and dorsal surface of the foot

A

Peroneal (common fibular) (actually divides into superficial and deep)

866
Q

Lambert-Eaton myathenic syndrome is a paraneoplastic syndrome to what type of cancer most commonly

A

Small cell lung cancer (small cells with neuroendocrine differentiation)

867
Q

In approximately 50% of patients with Lambert-eaton myasthenic syndrome, ______ is present

A

Underlying malignancy

868
Q

Lambert eaton myastenic syndrome is an autoimmune disorder with antibodies against _____

A

Presynaptc voltage gated calcium channel

869
Q

What would you expect on an MRI of Huntington disease

A

Enlargement of the frontal horns of the lateral ventricles and caudate atrophy

870
Q

N. Meningitidis has an outer cell membrane virulence factor called _____ which is primarily responsible for the severity of meningococcal disease

A

Lipo-oligosaccharide (LOS)

871
Q

Endotoxins bind to ______ on monocytic and dendritic cells and trigger release of inflammatory cytokies (IL 1, IL 6 and TNF alpha) which leads to endothelial damage, capillary leak, and hemorrhagic necrosis

A

Toll like receptor 4

872
Q

After thiamine infusion is started to treat Wernicke Korsakoff, what neurologic finding is most likely to persist despite treatment

A

Memory loss

873
Q

_____ is when patients with korsakoff syndrome are unsure of a fact so they filll in the memory gap with a fabricated stry that they themselves believe to be true

A

Confabulation

874
Q

The triad of Wernicke syndrome

A

Oculomtor dysfunction
Ataxia
Confusion

875
Q

The hallmarks of korsakof syndrome are ____ and _____

A

Permanent memory loss

Confabulation

876
Q

Narcolepsy results from the depletion of hypocretin (also known as orexin) secreting neurons in the ________ that are involved in maintaining wakefullness

A

Lateral hypothalamus

877
Q

Patients with narcolepsy experience shortened _____ and enter REM sleep almost immediately

A

Sleep latency

878
Q

Patients with narcolepsy commonly experience intrsions of REM sleep phenomena during sleep-wake transitions, including ____ (upon falling asleep) and ___ (upon awakening) hallucinations and sleep paralysis (inability to move immediately after wakening)

A

Hypnagogic

Hypnopompic

879
Q

What are 2 topical agents that can be used to treat neuropathic pain

A

Capsaicin

Lidocaine

880
Q

Name 4 non topical treatments that can be used for neropathic pain

A

Tricyclic antideperssants
SNRIs
Anticonvulsants (gabapentin)
Opiods (other 3 are first line, opiods are not)

881
Q

How do tricyclic antidepressents modulate pain transmission

A

Inhibit voltage gatd sodium channelsi n sensory nerve

Increase norepinephrine signaling in CNS

882
Q

The parasympathetic, preganglion neurons arise from ____ and ______

A

Cranial nerve nuclei (III, VII, IX, X)

Sacral spinal cord

883
Q

The parasympatheitc preganglionic neurons release ____

A

Acetylcholine

884
Q

The parasympathetic preganglionic neurons release acetylcholine on _____ receptors within the parasympathetic ganglia where?

A

Nicotinic

In or near the target organs

885
Q

Postganglionic parasympathetic neurons release _____

A

Acetylcholine

886
Q

Postganglionic parasympathetic neurons release acetylcholine on _____ receptors within the target organs

A

Muscarinic

887
Q

The sympathetic preganglionic neurons arise from ______

A

Thoracolumbar spinal cord

888
Q

The sympathetic preganglionic neurons release ____

A

Acetylcholine

889
Q

The sympathetic preganglionic neurons arise from the thoracolumbar spinal cord and release acetylcholine which binds post ganglionic ___ receptors in the sympathetic chain and prevertebral ganglia

A

Nicotinic

890
Q

Sympathetic postganglionic neurons release ______

A

Norepinephrine

891
Q

Postganglionic sympathetic neurons release norepinephrine, activating alpha/beta receptors within target organs with 2 exceptions: ____ and ____

A

Adrenan medulla

Sweat glands

892
Q

The chromaffin cells of the adrenal medulla release norepinephrine and epinephrine directly into circulation after being stimulated by the sympathetic nervous system how?

A

Acetylcholine release from sympathetic preganglionic neurons

893
Q

The preganglionic and postganglionic sympathetic neurons that supply eccrine sweat glands are both ____

A

Cholinergic

894
Q

In the brain, fluorinated anesthetics ____ vascular resistance and lead to a ______ in cerebral blood flow

A

Decrease

Increase

895
Q

Donepezil MOA

A

Acetylcholinesterase inhibitor (alzheimer tx)

896
Q

Alzheimer dementia involves dysfunction of ____ pathways in the brain

A

Cholinergic

897
Q

Acetylcholinesterase inhibitors may cause syncope due to enhanced parasympthetic tone that leads to ____ and ____ with reduced cardiac output

A

Bradycardia

Atrioventricular block

898
Q

Jugular foramen (________) syndrome is characterized by the dysfunction of cranial nerves IX, X, XI

A

Vernet

899
Q

______is a paired pigmented brainstem nucleus located in the posterior rostral pons near the lateral floor of the 4th ventricle. It functions as the principal site for norepinephrine synthesis in the brain and projects to virtually all parts of the CNS.

A

Locus ceruleus

900
Q

Voluntary muscle activity is mediated by the ____ tract

A

Corticospinal

901
Q

The _____ cortex of each hemisphere receives information about the contralateral visual field from the ipsalateral geniculate nucleus via the optic radiation

A

Striate

902
Q

The _____ gyrus ofthe striate cortex receives information from the upper retina (lower visual field)

A

Cuneus

903
Q

The ____ gyrus of the striate cortex receives information from the lower retina (upper visual field)

A

Lingual

904
Q

In PCA occlussion, the macula is spared because collateral blood is supplied by the _____ to the _____ pole which processes central visual information

A

Middle cerebral artery

Occipital

905
Q

The ____ gyrus is part of the parietal association cortex which integrates multisensory information to comprehend events and solve problems

A

Angular

906
Q

Damage to the angular gyrus classically results in ___ syndrome: characterized by agraphia, acalculia, finger agnosia, and left-right disorientation

A

Gerstmann syndrome

907
Q

The dorsal columns, carrying afferent vibration and proprioception fibers, are arranged topographically, medial fibers are from the ____ spinal level and lateral are from the ____ spinal levels

A

Lower

Higher

908
Q

The ___ fasciculus of the dorsal column, located medially , carries afferentinformation that enters the spinal cord below T6

A

Gracile

909
Q

The ____ fasciculus of the dorsal columns, located laterally, carries afferent information that enters the spinal cord above T6

A

Cuneate

910
Q

Frontotemporal dementia results in accumualtion of different neurotoxins including _____ and _____

A

Tau

TDP-43

911
Q

In frontotemporal dementia, abnormal ____ of TDP-43 leads to imunoreactive inclusions of TDP-43

A

Ubiquitination

912
Q

TDP-43 normally fuctions as a ______

A

Transcription inhibitor or DNA repair protein

913
Q

______ is a developmental anomaly characterized by hypoplasia/absence of the cerebellar vermis and cystc dilation of the 4th ventricle with posterior fossa enlargement

A

Dandy walker malformation

914
Q

The most common complication of SAH is arterial vasospasm which occurs due to the release of vasoconstrictive factors from damaged ______ in the subarachnoid space and the inability of damaged ______ to produce vasodilators (nitric oxide)

A

Erythrocytes

Endothelial cells

915
Q

3 neuronalpathologic features of alzheimers disease include neurodegeneration leading to neuronal loss and cerebral atrophy, extracellular ______, and intracellular ______

A
Beta amyloid plaques
Neurofibrillary tangles (tau protein agreggates)
916
Q

What are the 2 symptomtic treatment options for alzheimers (just mech of action)

A
NMDA receptor antagonist (memantine)
Cholinesterase inhibitors (donepezil, galantamine)
917
Q

Degeneration of _______ neurons in the basal forebrain contributes to memory loss and functional decline in alzheimer patients

A

Cholinergic

918
Q

What medications should be discontinued in alzheimers patients bc they can exacerbate cognitive dysfunction

A

Anticholinergic (tricyclic antidepressents)

919
Q

How are NMDA receptor antagonists helpful in treating alzheimers

A

Inhibit glutamate NMDA signaling –> prevent excitotoxicity (calclium overload) and subsequent neuronal apoptosis

920
Q

Neisseria meningitidis is transmitted via aerosolized droplets and are able to colonize the _____ due to the presene of specialized surface components (dimbriae, pili)

A

Nasopharynx

921
Q

Neisseria meningtidis causes meningitis by entering via the nasopharynx –> blood —> ______ —-> meninges

A

Choroid plexus

922
Q

Gingival hyperplasia in phenytoin treatment is due to increased expression of ______

A

Platelet derived growth factor (PDGF)

923
Q

When gingival _____ are exposed ot increased amounts of PDGF, they stimulate proliferation of gingval cells and alveolar bone

A

Macrophages

924
Q

If taken during pregnancy, phenytoin may cause ____ syndrome

A

Fetal hydantoin syndrome

925
Q

The most important biochemical abnormality noted in Alzheimers disease is decress in acetylcholine leves which occurs due to deficiency in _____

A

Choline acetyltransferase

926
Q

In alzheimers disease, the decline in acetylcholine is most notable in the nucleus ________ which participates in memory and cognition

A

Basalis of meynert

927
Q

Name the 3 branches directly off the aortic arch

A

Left common carotid
Left Subclavien
Right brachiocephalic

928
Q

The right common carotid artery branches from the _____

A

Brachiocephalic artery

929
Q

The L4 vertebral body lies on a line drawn between the highest points of the iliac _____ which can be visually identified and confirmed by palpation

A

Crests

930
Q

Patients with _____ occlusion usually present with contralateral hemiparesis and hemisensory loss involving mainly the face and upper limb (more than leg)

A

Middle cerebral artery

931
Q

In diabetic polyneuropathy, neuronal injury occurs due to accumulation of advanced glycosylation end products, ____, and other toxic substances that lead to derranced metabolism and increased oxidative stress

A

Sorbitol

932
Q

Diabetic microangiopathy affecting the _____ vessels can promote nerve ischemia

A

Endoneurial

933
Q

Length dependent axonapthy in diabetic polyneuropathy affects what nerves first

A

Longest nerves

934
Q

Small fiber injury is characterized by predominance of ____ symptoms (pain, paresthesia, allodynia)

A

Positive

935
Q

Large fiber inovlvemnet is characterized by predominance of ____ symproms (numbness, loss of proprioception and vibration sense, sensory ataxia, diminished ankle reflexes)

A

Negative

936
Q

Several months-years after brain infarction, the necrotic area appears as a cystic cavity surrounded by a wall composed of dense fibers formed by what cells

A

Astrocytes

937
Q

___ disease is a rare autosomal recessive disorder most often identfied in individual aged 5-40 with decreased secretion of copper into the biliary system resulting in movement abnormalities and psych symptoms

A

Wilson

938
Q

Wilson diease is a autosomal recessive disorder with a mutation in ______

A

ATP7B

939
Q

Wilson disease is an auto recessive disorder with a mutation in ATP7B which hinders intracellular hepatocyte copper transport causing reduced formation/secretion of ______ (the major extracellular copper transport protein)

A

Ceruloplasmin

940
Q

Almost all patiens with wilson disease have ________ which are green/brown copper deposits in the Descemet membrane of the cornea and can be detected with a slit lamp examination

A

Kayser-Fleischer rings

941
Q

Diagnosis of Wilson disease can be confirmed by presense of low serum ceruoplasmin, elevated urinary ___ excretion, and elevated hepatic ____ content on liver biopsy

A

Copper

Copper

942
Q

How can Wilson disease be treated

A

Chelators (D-penicillamine, trientine)

Zinc (interferes with copper absorption)

943
Q

What is the result of a charcot-bouchard aneurysm rupture

A

Intracerebral hemorrhage

944
Q

What is the result of a saccular aneurysm rupture

A

Subarachnoid hemorrhage

945
Q

The gag reflex is mediated by afferents predominantly from the _____ nerve and efferents from the ___ nerve

A

Glossopharyngeal (CN IX)

Vagus (x)

946
Q

Petellar reflex tests what nerve roots

A

L2-l4

947
Q

Sensation to anteromedial thigh and medial shin is innervated by what nerve roots

A

L2-L4

948
Q

What nerve roots are tested in achilles reflex

A

S1

949
Q

What nerve roots innervated sensation to perineum

A

S2-S4

950
Q

What nerve roots innervated hip flexion (iliopsoas), hip adduction, knee extension (quadricep)

A

L2-L4

951
Q

What nerve roots innervate hip extension (glut max) and plantarflexion (gastrcnemius)

A

S1

952
Q

What nerve roots are tested with the anocutaneous reflex

A

S2-S4

953
Q

What nerve roots innervated sensation to the posterior calf, sole, and lateral foot

A

S1

954
Q

What nerve roots innervted sensation to lateral shin and dorsum of foot

A

L5

955
Q

What nerve roots innervated foot dorsiflexion and inversion (tibialis anterior), foot eversion (peroneus), and toe extension (extensor hallucis and digitorum)

A

L5

956
Q

Injury to what nerve roots will cause urinary or fecal incontinence and sexual dysfunction

A

S2-S4

957
Q

What nerve innervates the glutesus medius, gluteusminimus, and tensor fasciae latae muscles

A

Superior gluteal nerve

958
Q

The glut medius, glut minimus, and tensorfasciae latae function to stabilize th pelvis and ___ the thig

A

Abduct

959
Q

What is a positive trendlenburg sign

A

Pelvis sags toward unaffected (contralateral) side when the patient stands on the affected (ipsilateral) leg

960
Q

A patient with weakness to what muscles will have a positive trendelenburg sign

A

Gluteus medius and glutes minimus

961
Q

What is a gluteus medius lurch

A

When a patient with gluteus medius and gluteus minimis weakness leans toward the affected side when walking to compnesate for hip drop

962
Q

The temporal bone contains the vestibularochlear nerve as well as what other cranial nerve which enters at the internal auditory meatus and travels through the internal auditory canal with the vestibulocochlear nerve

A

CNVII (facial)

963
Q

What cause of meningitis causes acute onset fever, headache, altered mental status, and focal neurologic deficits or seizures as well as temporal lobe edema

A

Herpes simplex virus type 1

964
Q

What are the CSF findings in patients with meningitis due to herpes simplex virus 1

A

Normal glucose
Elevated protein
Elevated lymphocytes and erythrocytes (due to hemorrhagic inflammation in temporal lobes)

965
Q

In the CNS the phagocytic macrophages/glia are recruited more slowly due to the BBB, mylein producing oligodendrocytes also beome inactive or undergo apoptosis and do not asist in phagocytosis. This results in the persistance of what for months-years following ischemic injury

A

Myelin debris

966
Q

How is tetanus diagnosed

A

Clinical diagnosis

967
Q

Why are blood cultures of tetanus not helpful for diagnosis

A

C. Tetani only grows at the inoculation site, the toxins then spread and cause the symptoms

968
Q

What vascular changes result in diabetic neuropathy

A

Hyalinization of the endoneurial arterioles —> ischemic nerve damage

969
Q

______ is a compression mononeuropathy of the lateral femoral cutaneous nerce at the inguinal ligament, typically caused by tight clothing or injury dduring surgery

A

Meralgia paresthetica

970
Q

Meralgia paresthetica presents with pain, paresthesia and numbness over what distribution

A

Lateral thigh above the knee

971
Q

A patient with a ring enhancing lesion in the temporal lobe who has been puling on her ear recently likely is infected with a pathogen that entered her brain through what structure

A

Mastoid air cells (otitismedia that spread)

972
Q

Frontal lobe abscesses are generally due to direct spread of a pathogen from what structures

A

Ethmoid or frontal sinus

973
Q

What occur as a result of compression of spinal nerve roots and typically present with neck or arm pain and motor/sensory deficits

A

Cervical radiculopathy

974
Q

Cervical radiculopathies result from what 2 ways

A

Spinal sponylosis

Vertebral disc herniation

975
Q

What is spinal spondylosis

A

Aging –> degeneration of vertebral bodies, discs, joints –> osteophye formation –> narrows neuronal formamina

976
Q

A subdural hematoma is due to a rupture of _____

A

Cortical bridging veins

977
Q

The cells that are typically affected first by hypoxia are the _____ neurons in the ____ which can be damaged by iscemia in as little as 3 min

A

CA1 pyramidal

Hippocampus

978
Q

In addition to the hippocamus, the cerebellar ____ cells and neocortex _______ neurons are also highly susceptible to damage if ischemia lasts for 5-10 min

A

Purkinje

Pyramidal

979
Q

Cerebellar ataxia, telangiectasia and increased risk of sinopulmonary infections constitute a characteristic triad of wha hereditary disease

A

Ataxia telangiectasia

980
Q

Ataxia telangiectasia causes an immune deficiency that primarily manifests as a ___ deficiecy predisposing the patient to infections of the upper and lower airways

A

IgA

981
Q

In ataxia telangiectasia, the autosomal recessive gene mutation in the ATM gene is responsible for ____

A

DNA break repair

982
Q

In MS, activated CD8 T cells release cytotoxi granules that injure _____

A

Oligodendrocytes

983
Q

In MS, B cell recruitment leads to the formation of antibodies that activate complement and facilitate _____ breakdown

A

Myelin

984
Q

Diagnosis of MS is largely clinical but supported by the pressence of ____ lesions on MRI

A

T2

985
Q

Are oligoclonal bands specific or sensitive for dx of MS

A

Sensitive

986
Q

Blepharospasm, the second most common focal dystonia is what

A

Involuntary forcible closre of the eyelids

987
Q

Hydrocephalus is a common complication of subarachnoid hemorrhage due to what

A

Blood in subarachnoid space can acutely obstruct and impair absorption of cerebral spinal fluid by the arachnoid granulations

988
Q

What are 3 common findings of TB meningitis

A

Gelatinous exudate at basal portion of brain
Multiple bilateral brain infarcts
Hydrocephalus (can cause ventriculomegaly)

989
Q

What is an autopsy likely to reveal in a patien with HSV1 encephalitis

A

Unilateral temporal lobe inflammation

990
Q

_____ syndrome presets as a patient with quadriplegia and speechlessness with preserved consciousness and eye mvements

A

Locked in syndrome

991
Q

Locked in syndrome can be caused by ischemic injury to ____

A

Bilateral ventral pons

992
Q

In locked in syndrome horizontal eye movements are absent but why are vertica eye movements and eyelid elevation spared

A

They are controlled in rostral midbrain, not in ventral pons

993
Q

Preserved conscoiusness in locked in syndrome is due to _______ being spared

A

Midbrain reticular formation

994
Q

Neural tissu with neurons with shrunken nuclei and eosinphilic cytoplasm lacking Nissl bodies indicates what type of injury

A

Irreversible ischemic injury

995
Q

Describe a pyknotic nucleus

A

Shrunk and basophilic with loss of nucleolus

996
Q

Subacute cerebellar degeneration is a paraneoplastic syndrome seen in smal cell lung cancer via what mechanims which damage purkinje neurons

A

Anti-Yo, anti- P/Q and anti-Hu auto antibodies

997
Q

On macroscopic examination, ______ are cystic or partialy solid with cyst being filled with a brownish yellow, viscocus fluid that resembles machine oil due to the presence of protein and cholesterol crystals

A

Adamantinomatous craniopharyngioma

998
Q

Adamantinomatous craniopharyngioma are found in children and typically located in the ____

A

Suprasellar region

999
Q

In adamantinomatous craniopharyngioma _______ of the cysts is highly characteristc and may be deteced on euroimaging

A

Dystrophic calcification

1000
Q

An adamantinomatous craniopharyngioma, on light microscopy, will reveal cysts lined with cords/nests of _____ with peripheral palisading and internal areas of lamellar ______

A

Stratified squamous epithelium

Wet keratine

1001
Q

Craniopharyngioas are derived from remnants of the _____

A

Rathkes pouch

1002
Q

Abusive head trauma (shaken baby syndrome) results in what type of hemorrage

A

Subdural (tearing of bridging veins)

1003
Q

_______ due to rupture of congested retinal veins are highly suggestive of abusive head trauma(shaken baby syndrome)

A

Retinal hemorrhages

1004
Q

Patient with progressive headaches has an enhancing ventricular mass on MRI is consistent with what diagnosis

A

Ventricular ependymoma

1005
Q

What histological finding an confirm the diagnosis of an ependymoma

A

Perivascular pseudorosettes

1006
Q

How can cocain cause myocardial infarction

A

Coronary artery vasospasm

Increased platelet aggregation

1007
Q

Cocaine MOA

A

Inhibits presynaptic reuptake of monoamines

1008
Q

An adequate antidepressant trial is generally considered to be at least how long?

A

4-6 weeks

1009
Q

What distinct features of neuroleptic syndrome differentiate it from serotinn syndrome

A

Diffuse rigidity (lead pipe) and hyporeflexia seen in NMS

1010
Q

What distinct features seen in serotonin syndrome diferentiate it from neuroleptic malignant syndrome

A

Clonus and hyperreflexia are seen in serotonin syndrome

1011
Q

What precipitates neuroleptic malignant syndrome

A

Dopamine antagonist

1012
Q

MOA: bupropion

A

Inhibits reuptake of norepinephrine and dopamine

1013
Q

What medication is contraindicated in patients with seizure disorders or current or prior diagnosis of bulimia or anorexia nervosa due to increased risk of seizures

A

Buproprion

1014
Q

Withdrawals from what substance produce symtpoms of increased apetite, hypersomnia, intense psychomotor retardation, severe depression and can be accompnied by vivid dreams

A

Stimulants (amphetamines, cocaine)

1015
Q

What dissociative disorder involves either or both: depersonalization (detachment, unreality of self) and derealization (detachment, unreality of surroundings)

A

Deprsonalization/derealization disorder

1016
Q

What dissociative disorder involves the inability to recall personal information, usually of a traumatic or stressful nature

A

Dissociative amnesia

1017
Q

What dissociative disorder involves framentation into 2 or ore distinct personalities and discontinuity in identity and personal agency

A

Dissociative identity disorder

1018
Q

Second generation antipsychotic medications are associated most with what adverse effects

A

Metabolic

1019
Q

How should patients on second generation antipsychotics be monitored

A

BMI
Fasting glucose and lipids
Blood pressure
Wais circumference

1020
Q

Within second generation antipsychotics, which medications carry the most risk for metabolic adverse effects

A

Olanzapine

Clozapine

1021
Q

Chronic ethanol use causes downregulation of _____ receptors

A

GABA

1022
Q

What is the most common initial symptom of alcohol withdrawal

A

Tremor (can start as early as 6 hours after last drink)

1023
Q

If a patient has 5 or more symptoms of major depressive disorder lasting more than 2 weeks following a precipitating event (ie losing their job) what is the diagnosis

A

Major depressve disorder (adjustment disorderis the diagnosis when patient does not have 5 of the symptoms meeting major depressive disorder diagnosis)

1024
Q

What is the diagnosis of a patient who has a pervasive pattern of distrust and suspiciousness beginning in early adulthood and occurig in a variety of settings including believes being exploited and deceived by others, interprets benign comments and events as threats, bears grudges, and questions loyalty of partner without justification (no fixed delusions and no other psychotic symptoms)

A

Paranoid personality disorder

1025
Q

A child who is previously meeting developmental milestones and now has dramatic regression of speech and motor milestones accompanied by repetitive hand movements is concerning for what dignosis

A

Rett syndrome

1026
Q

Rett syndrome is a sporadic, X-linked genetic disorder in what gene

A

MECP2

1027
Q

Does Rett syndrome cause neurodegeneration?

A

No, neuropathology is consitant with arrested brain development

1028
Q

How does bulimia nervosa differ from binge eating disorder

A

Bulimia nervosa involves inappropriate comensatory behavior (fasting, purging) while binge eating disorder does not

1029
Q

Of risk factors for suicide, what is the strongest single factor that is most predictive of a completed suicide

A

History of an attempted suicide

1030
Q

Cocaine MOA

A

Inhibits presynaptic reuptake of monoamines

1031
Q

An adequate antidepressant trial is generally considered to be at least how long?

A

4-6 weeks

1032
Q

How does bulimia nervosa differ from binge eating disorder

A

Bulimia nervosa involves inappropriate comensatory behavior (fasting, purging) while binge eating disorder does not

1033
Q

Does Rett syndrome cause neurodegeneration?

A

No, neuropathology is consitant with arrested brain development

1034
Q

Rett syndrome is a sporadic, X-linked genetic disorder in what gene

A

MECP2

1035
Q

A child who is previously meeting developmental milestones and now has dramatic regression of speech and motor milestones accompanied by repetitive hand movements is concerning for what dignosis

A

Rett syndrome

1036
Q

What is the diagnosis of a patient who has a pervasive pattern of distrust and suspiciousness beginning in early adulthood and occurig in a variety of settings including believes being exploited and deceived by others, interprets benign comments and events as threats, bears grudges, and questions loyalty of partner without justification (no fixed delusions and no other psychotic symptoms)

A

Paranoid personality disorder

1037
Q

If a patient has 5 or more symptoms of major depressive disorder lasting more than 2 weeks following a precipitating event (ie losing their job) what is the diagnosis

A

Major depressve disorder (adjustment disorderis the diagnosis when patient does not have 5 of the symptoms meeting major depressive disorder diagnosis)

1038
Q

What is the most common initial symptom of alcohol withdrawal

A

Tremor (can start as early as 6 hours after last drink)

1039
Q

Chronic ethanol use causes downregulation of _____ receptors

A

GABA

1040
Q

Within second generation antipsychotics, which medications carry the most risk for metabolic adverse effects

A

Olanzapine

Clozapine

1041
Q

How should patients on second generation antipsychotics be monitored

A

BMI
Fasting glucose and lipids
Blood pressure
Wais circumference

1042
Q

Second generation antipsychotic medications are associated most with what adverse effects

A

Metabolic

1043
Q

What dissociative disorder involves framentation into 2 or ore distinct personalities and discontinuity in identity and personal agency

A

Dissociative identity disorder

1044
Q

What dissociative disorder involves the inability to recall personal information, usually of a traumatic or stressful nature

A

Dissociative amnesia

1045
Q

What dissociative disorder involves either or both: depersonalization (detachment, unreality of self) and derealization (detachment, unreality of surroundings)

A

Deprsonalization/derealization disorder

1046
Q

Withdrawals from what substance produce symtpoms of increased apetite, hypersomnia, intense psychomotor retardation, severe depression and can be accompnied by vivid dreams

A

Stimulants (amphetamines, cocaine)

1047
Q

What medication is contraindicated in patients with seizure disorders or current or prior diagnosis of bulimia or anorexia nervosa due to increased risk of seizures

A

Buproprion

1048
Q

MOA: bupropion

A

Inhibits reuptake of norepinephrine and dopamine

1049
Q

What precipitates neuroleptic malignant syndrome

A

Dopamine antagonist

1050
Q

What distinct features seen in serotonin syndrome diferentiate it from neuroleptic malignant syndrome

A

Clonus and hyperreflexia are seen in serotonin syndrome

1051
Q

What distinct features of neuroleptic syndrome differentiate it from serotinn syndrome

A

Diffuse rigidity (lead pipe) and hyporeflexia seen in NMS

1052
Q

Of risk factors for suicide, what is the strongest single factor that is most predictive of a completed suicide

A

History of an attempted suicide