Neurological Issues and Disorders Flashcards

1
Q

Tic Disorders

A

brief, abrupt, non-purposeful movements or utterances

most common is tourette syndrome–refer to neurology

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2
Q

What is the normal onset of tics?

A

between 6 and 12 years of age

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3
Q

What are causes of tics?

A

unknown–possibly familial predisposition

associated with medications such as methylphenidate and amphetamines

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4
Q

Copropaxia

A

obscene gestures

- seen with complex motor tics

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5
Q

coprographia

A

obscene writing

- seen with complex motor tics

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6
Q

Vocal tics

A

oropharyngeal, nasopharyngeal or laryngeal sounds
consonants or syllables
meaningful or nonsense words or phrases
coprolalia (obscene speech)
palilalia (repeating one’s own words) and echolalia (repeating anothers words)

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7
Q

Complex motor tics

A

involves vocal tics and simple motor tics

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8
Q

Neurofibromotisis

A

von Recklinghausen disease
a neurocutaneous syndrome characterized by numerous cafe-au-lait spots on the body and nerve tumors on the skin and in body
progressive disorder that does not affect intelligence
autosomal dominant, present in a first degree relative

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9
Q

What are signs and symptoms of neurofibromatosis?

A

multiple cafe-au-alit spots

seizures

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10
Q

What are the diagnostic criteria for neurofibromatosis?

A

must have at least 2 of the following:

  • six more more CLS spots >5 mm in prepubertal child OR >15 mm in post pubertal child
  • 2 or more cutaneous neurofibromas (flat, varying in size)
  • axillary or inguinal freckling
  • 2 or more lisch nodules in eyes (looks like black dots)
  • distinctive osseous lesions
  • autosomal dominant, present in 1st degree relative
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11
Q

Febrile seizures

A

seizures occurring during the course of and as a result of fever with peak incidence of 1-3 years old

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12
Q

If a seizure occurs greater than 24 hours after a fever then it most likely means?

A

infection

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13
Q

Risk factors for febrile seizures

A

family history of a seizure disorder, tobacco use by mother during pregnancy, neonatal hospitalization >28 days, frequent infections in 1st year of life

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14
Q

Majority of febrile seizures are_____

A

tonic clonic

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15
Q

What is the recurrence rate for febrile seizures?

A

after 1: 30% for a 2nd

after 2: 50% for a 3rd

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16
Q

Partial seizures

A

involves one hemisphere

Simple partial: no LOC, a variety of other symptoms (motor, autonomic, and sensory)

Complex partial: impaired consciousness–staring >20 seconds before, during, or after symptoms

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17
Q

Generalized seizures

A

bilateral, involving both hemispheres

types: absence (petit mal), tonic, tonic-clonic (grand mal), atonic

18
Q

Absence seizure

A

petit mal
brief staring episodes (10-20 seconds)–may smack lips, blink eyes, stare ahead
onset and termination are very brief
usually benign in childhood

19
Q

Tonic seizure

A

sudden increase in muscle tone producing postures
consciousness is usually partially or completely lost
postictal alternation of consciousness is usually brief, may last several minutes

20
Q

Tonic clonic seizure

A

grand mal

sudden LOC with arrested respirations
clonic phase involves increased muscle tone followed by bilateral rhythmic jerks lasting 2-3 minutes, followed by flaccid coma
urinary or fecal incontinence may occur
postictal state is characterized by deep sleep for up to an hour, headache, disorientation, muscle discomfort, nausea–can last for a minute to hours

21
Q

Atonic seizure

A

sudden loss of muscle tone

may result in head drop or falling to the ground

22
Q

Signs and symptoms of a brain tumor in an infant

A

increased head circumference, tense, bulging fontanel without fever
irritability
head tilt
loss of developmental milestones

23
Q

Signs and symptoms of a brain tumor in a child

A

headache–worst in the morning followed by vomiting, usually increase in frequency

Abnormal neurological or ocular findings:
ataxia, hemiparesis, cranial nerve palsies
somnolence 
seizures
head tilt, FTT, diabetes insipidus
papilledema 
loss of fine motor control 
positive babinski sign 
behavior changes
24
Q

Infratentorial, brainstem tumors predominate what age group?

A

4-11 year olds

25
Q

When ordering diagnostic tests on someone with a brain tumor, what test should you approach with caution?

A

LP

26
Q

Migraines are due to _______

A

dilation and excessive pulsation of the beaches of the external carotid artery

27
Q

Classic migraine

A

with aura

>10 years old

28
Q

Common migraine

A

without aura

29
Q

Confusional migraine

A

more common in younger children
period of confusion and disorientation followed by vomiting and deep sleep, waking feeling well
headache may not be described

30
Q

Abdominal migraine

A

episodic abdominal pain with nausea, vomiting followed or accompanied by headache

31
Q

Prophylactic pharmacologic therapy for migraines

A

**prophylactic therapy if attacks occur more than 3-4 times per month, or if migraines interfere with daily functioning or school

NSAIDS
propranolol (inderal)
amitriptyline (elavil)
topiramate (topamax)
imipramine (tofranil)
verapamil (calan)
32
Q

Pharmacologic management for acute migraine attack

A

Tylenol or ibuprofen taken right away (7.5-10 mg/kg dose in younger children, may use up to 800 mg/dose in older teens)

  • *–triptans for adolescents
  • *maxalt or imitrex nasal for children ages 6-11

avoid in children at risk for heart disease

33
Q

What are the 4 mechanisms of headache pain?

A
  1. vascular dilation: cranial artery distention (migraine, fever)
  2. muscular contraction: head and neck muscle contraction (tension)
  3. traction: space occupying lesion (tumor, mass, abscess, hematoma, increased ICP)
  4. inflammation: infection (meningitis, sinuses, teeth, encephalitis)
34
Q

Afebrile headache differentials

A
subarachnoid hemorrhage
intraparenchymal hemorrhage 
postictal headache
cerebral ischemia
severe hypertension
space-occupying condition (brain tumor, hydrocephalus)
acute dental disease
acute glaucoma, inflammatory disease of the eye/orbit
35
Q

Febrile headache differentials

A

meningitis
brain abscess or other intracranial infection
encephalitis
sinusitis
associated infection: strep throat, mono, influenza, rubeola

36
Q

Meningitis

A

viral is more common in infants
bacterial only occurs in up to 2% –infants between 6-12 months old are at highest risk and 90% of cases occur in children between 1 month-5 years

37
Q

Signs and symptoms of meningitis

A

Newborns/infants: mimics septicemia, temp instability, irritability, poor feeds, lethargy, vomiting, bulging fontanel, no stiff neck

Older infants and children: N/V, irritability and confusion, headaches, back pain, nuchal rigidity, hyperesthesia, cranial nerve palsy, ataxia, photophobia

38
Q

Kerning’s sign

A

if lift Knee up, head lifts up

flexion of hip at 90 degrees, pain on extension of leg

39
Q

Brudzinski’s sign

A

if lift head up, knee comes up

involuntary flexion of legs when neck is flexed

40
Q

CSF analysis of meningitis

A

cloudy
WBCs present
increased protein
decreased glucose

41
Q

Name the cranial nerves, what their major functions are, and what type they are (sensory, motor, or both)

A
  1. Olfactory–smell, S
  2. Optic–vision, S
  3. Oculomotor–most EOMS, opening eyelids, papillary constriction, M
  4. Trochlear–down and inward eye movement, M
  5. Trigeminal–muscles of mastication, sensation of face, scalp, cornea, mucus membranes, and nose, B
  6. Abducens–lateral eye movement, M
  7. Facial–move face, close mouth and eyes, taste anterior, saliva, tear secretion, B
  8. Acoustic–hearing and equilibrium, S
  9. Glossopharyngeal–phonation, gag reflex, carotid reflex, swallowing, taste posterior, B
  10. Vagus–talking, swallowing, general sensation from carotid body, carotid reflex, B
  11. Spinal accessory–movement of trapezius and sternomastoid muscles (shrug shoulders), M
  12. hypoglassal–moves the tongue, M

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