neuro Flashcards

1
Q

common migraine preventative meds

A

cyproheptadine, topamax

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2
Q

most common malignant brain tumor of childhood

A

medulloblastoma

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3
Q

headache, ataxia, obstructive hydrocephalus

A

medulloblastoma

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4
Q

endocrinopathies, behavior changes, visual disturbances

A

craniopharyngioma
calcification in sella turcia
tx: surgery, radiation

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5
Q

assoc with optic nerve glioma

A

NF

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6
Q

cranial bruit in neonate

A

vein of Galen malformation

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7
Q

causes of acute ataxia

A

vaccinations
post viral
tox

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8
Q

recurrent resp infections, eye pigmentation, CNS findings

A

ataxia telangiectasia
AR
inc risk of lymphoma/leukemia

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9
Q

clumsy gait, elevated plantar arch, no LE DTRs, cardiomyopathy

A

Friedrich ataxia

AR

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10
Q

meds that cause ataxia

A

AEDs

thallium

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11
Q

meds that cause tremor

A

amphetamines
VPA
phenothiazines
TCAs

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12
Q

chorea, hypotonia, emotional lability

A

Huntingon chorea

AD

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13
Q

difference with juvenile Huntington

A

present with rigidity

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14
Q

tics

A

repetitive, improve/disappear with purposeful movement, can be suppressed

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15
Q

stereotypies

A

rocking, hand flapping

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16
Q

tx Tourette’s

A

habit reversal training

rx only if interfering with daily activities

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17
Q

fever, abrupt onset weakness and decreased reflexes

A

transverse myelitis
usually spontaneous recovery
pain on palpation of spinal cord
need MRI with gad

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18
Q

steroids in spinal cord compression vs spinal trauma

A

dex for compression

methylpred for trauma

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19
Q

tx Guillain Barre

A

IVIG, pheresis

20
Q

tx myasthenia

A

pyridostigmine
pheresis, plasma exchange
thymectomy can be curative in children

21
Q

ID in duchennes

A

often present, but usually mild

22
Q

dx duchennes

A

genetic testing for Xp21

CK always elevated even before sx

23
Q

inheritance duchennes

A

Xlinked
frequent spontaneous mutation
CK level can be elevated in female carriers

24
Q

cause of death in duchennes

A

heart failure

respiratory failure

25
muscles with slow relaxation after contraction, distal muscle wasting, endocrinopathies
myotonic muscular distrophy AD CK levels may be normal
26
dx myotonic muscular dystrophy
muscle biopsy
27
risk factors for recurrence of febrile seizure
low fever at time of sz young age family hx short period of time between fever and seizure
28
percent of febrile sz children who develop epilepsy
5%
29
3 second spike and wave EEG
absence seizure
30
what maneuver to induce absence seizure
hyperventilation
31
tx absence seizure
ethosuximide | lamictal, VPA
32
VPA SEs
cytopenias | liver and pancreas dysfn
33
myoclonic jerks on waking, GTCs, absence seizures
juvenile myoclonic epilepsy
34
EEG findings in JME
none
35
tx JME
VPA, keppra
36
hypsarrhythmia EEG
infantile spasms
37
assoc with infantile spasms
tuberous sclerosis
38
tx infantile spasms
ACTH | vigabatrin
39
prognosis of infantile spasms
if developmental delay prior, poor prognosis
40
centrotemporal spikes and slow waves EEG
benign rolandic epilepsy
41
seizures at night, facial seizures (usually unilateral sensory involvement), aware but unable to speak
benign rolandic epilepsy
42
inheritance benign rolandic epilepsy
dominant
43
when to tx benign rolandic epilepsy
only after 3+ seizures
44
when to attempt weaning of AEDs
if sz free for 2 years
45
most common risk factor for developing CP
perinatal infection
46
spastic quadriplegia with dystonia and strange movements
dyskinetic cerebral palsy
47
stroke, elevated lactate, SNHL
mitochondrial disorder