Neurology Flashcards

1
Q

Unilateral pupillary dilation
Compression of CN3

A

Uncal herniation

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2
Q

Headache that gets worse when lying flat and/or with Valsalva
Papilledema
Optic disc atrophy
Blindness

A

Idiopathic intracranial hypertension

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3
Q

Management for idiopathic intracranial hypertension

A

Acetazolamide
Diuretics

Seriously LP
CSF shunt
Steroids

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4
Q

Most common childhood malignant brain tumor

A

Medulloblastoma

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5
Q

Brain tumor
Headache
Ataxia
Obstructive hydrocephalus

A

Medulloblastoma

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6
Q

Headache
Vomiting
Ataxia
Afebrile
Head tilt
Torticollis

A

Infrantentorial/posterior fossa tumors

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7
Q

Headache
Seizure
Hemiparesis

A

Supratentorial tumors

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8
Q

Endocrinopathies
Behavioral changes
Visual disturbances
3rd ventricle obstruction
Hydrocephalus
Calcification in the sella turcica

A

Craniopharyngioma

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9
Q

Sinusitis
Headache
Vomiting
Focal neuro deficits
Brain enhancing lesion

A

Brain abscess

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10
Q

Neonate
Cranial bruit
Hydrocephalus
CHF

A

Vein of Galen malformation

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11
Q

Red blotches on skin/eyes
CNS effects
Intellectual disability
Decreased IgA and IgG
Respiratory tract infections
Hodgkin’s lymphoma (elevated AFP)
Autosomal recessive

A

Ataxia Telangiectasia

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12
Q

Slow/clumsy gait
Decreased strength
Decreased reflexes
Elevated plantar arch
Cardiomyopathy/CHF
Glucose intolerance (DM)
Autosomal recessive

A

Friedreich ataxia

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13
Q

Clumsiness
Distal muscles weakness
Absence of Lower DTRs
High plantar arch
Weakness
Distal calf muscle atrophy
Autosomal dominant

A

Charcot-Marie-Tooth disease

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14
Q

Syndeham chorea

A

Acute rheumatic fever

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15
Q

Chorea
Hypotonia
Emotional lability
Autosomal dominant

A

Huntington chorea

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16
Q

Treatment for chorea

A

Supportive
Haloperidol

Fluphenazine
Risperidone
Tetrabenazine

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17
Q

Neck hyperextension
Decreased extraocular movement

Treatment

A

Acute dystonic reaction

Benadryl

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18
Q

Specific repetitive movement
Improves/disappears with purposeful movement
Voluntarily suppressed

A

Tic

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19
Q

Weakness
Paresthesias
Localized back pain
Fever
Reduced LE sensation and bowel/bladder tone

Treatment

A

Epidural abscess

Abx
Steroids
Surgical decompression

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20
Q

Virus
Fever
Weakness then hypertonia/hyperreflexia
Bowel/bladder dysfunction
Lymphocytic infiltration and demyelination

A

Acute transverse myelitis

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21
Q

Treatment for extrinsic spinal cord lesion

A

High dose IV dexamethasone

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22
Q

Degeneration of anterior horn cells
Only motor dysfunction
Infancy
Poor suck
Tongue fasciculations

A

Spinal muscular atrophy (SMA) type 1

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23
Q

Minimal vertebral opening
Spinal cord and nerves intact
Asymptomatic

A

Spina bifida occulta

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24
Q

Larger vertebral opening
Herniation if CSF and meninges
Intact spinal cord
Asymptomatic

A

Meningocele

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25
Widely split vertebral opening Herniation of CSF, meninges, spinal cord Paralysis Ortho and uro problems
Myelomeningocele
26
Steroid choice for spinal trauma
IV methylprednisolone 30mg/kg
27
Decreased forehead wrinkling Decreased smiling on affected side Treatment
Bell’s palsy Supportive Prednisone +/- acyclovir/valacyclovir
28
Increase protein in CSF with normal cell count Campylobacter jejuni Proximal muscle weakness
Guillain barre syndrome
29
Descending paralysis Poor suck Ptosis Constipation, urinary retention Disconjugate gaze Diplopia Dysphagia Dysarthria
Botulism Blocks ACh release
30
Proximal muscle weakness worsens with activity Ptosis Thymoma
Myasthenia gravis ACh receptor antibodies
31
Diagnosis and management of myasthenia gravis
Tensilon test - edrophonium (ACh inhibitor) Pyridostigmine (ACh inhibitor) PLEX Prednisone Thymectomy
32
X-linked recessive Absence of dystrophin protein Gower sign Pseudohypertrophied calves Elevated CPK Xp21 abnormality
Duchenne muscular dystrophy
33
Autosomal dominant Striated and smooth muscle affected Distal muscle weakness Slow relaxation after contraction
Myotonic muscular dystrophy
34
Marcus Gunn phenomenon
Abnormal interaction of trigeminal and oculomotor nerves
35
Seizures 6mo to 6 yr Most common Febrile illness
Febrile seizures
36
Simple febrile seizure
Generalized < 15 min 1 episode in 24 hr
37
Complex febrile seizure
Focal > 15 min > 1 episode in 24 hr
38
3 hz per second spike and wave
Absence seizure
39
Seizure caused by hyperventilation
Absence seizure
40
Treatment for absence seizure
Ethosuximide Lamotrigine Valproic acid
41
Side effects of valproic acid
Thrombocytopenia Elevated LFTs and pancreatic enzyme levels Teratogenic (meningomyelocele) Hyperammonemia
42
Side effect of Topiramate
Glaucoma
43
Side effect of Lamotrigine
Steven Johnson syndrome
44
Side effect of phenytoin
Teratogenic (fetal hydantoin syndrome)
45
Myoclonic jerks of bilateral UE upon awakening Generalized tonic clonic seizure Absence seizure in 1/3 of patients
Juvenile Myoclonic epilepsy
46
4-6 hz polyspike and wave discharges
Juvenile Myoclonic epilepsy
47
Infantile spasms Hypsarrhytmia (inferictal on EEG) Developmental delay 3-9 mo Repetitive flexing of head, trunk, extremities
Infantile spasm (west syndrome)
48
Periventricular or cortical tubers Infantile spasms, seizures Cardiac rhabdomyomas Renal angiomyolipoma Shagreen patches Ash leaf spots Angiofibromas Autosomal dominant
Tuberous sclerosis
49
Treatment for tuberous sclerosis
ACTH Vigabatrin
50
Treatment for simple partial complex seizure
Carbamazepine
51
Twitching, grunting, tongue rolling, choking sensation Often cannot speak if occurs during wakefulness Most common type of partial seizure in childhood Autosomal dominant Biphasic focal centrotemporal spikes and slow waves on EEG
Benign Rolandic epilepsy (Benign childhood epilepsy with centrotemporal spikes) Spontaneous remission by 12 yo
52
Most common risk factor for cerebral palsy in premature newborns
Perinatal infection
53
Spastic diplegic CP
Bilateral spasticity of legs Delayed walking Tip toe walking g Normal cognition No Seizures
54
Spastic hemiplegic CP
Ipsilateral spasticity 1/4 cognitively impaired
55
Spastic quadriplegic CP
Increased tone in all extremities Intellectual disability Seizures
56
Dyskinetic (athetoid) CP
Spastic quadriplegia + Dystonic and strange movements
57
Ataxic CP
Hypotonia Delay in motor and language milestones Retention of primitive reflexes and or hyperactive reflexes
58
Most common cause of hemorrhagic stroke in children
AV and cavernous malformations
59
Next diagnostic step after presented with CVA on head CT
Cerebral angiography
60
Stroke Lactic acidosis Sensorineural deafness Best diagnostic study
MELAS Mitochondrial encephalopathy, Lactic Acidosis, Stroke-like episodes Molecular analysis of mitochondrial DNA
61
Prophylaxis for cluster headache
Verapamil
62
1st line treatment for infantile spasms
ACTH Prednsolone Vigabatrin
63
Prophylaxis for migraine headache
Topiramate
64
Impaired upward gaze Dilated pupils Better reactivity to accommodation than light Retraction/conversion nystagmus with lid retraction Compression or infiltration of midbrain rectum (pineal tumors)
Parinaud syndrome