Neuro Flashcards

1
Q

TRIAD of West syndrome

A

Infantile epileptic spasm
developmental regression
EEG = hypsarrhythmia

between 2-12mos

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2
Q

Severe myoclonic epilepsy of infancy

A

Dravet syndrome

start: focal febrile status epilepticus or focal febrile seizures
later: manifests myoclonic and other seizure types

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3
Q

Early infantile epileptic encephalopathy

A

Ohtahara syndrome
manifests tonic seizures and usually caused by brain malformations or syntaxin binding protein 1 mutations

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4
Q

triad of Lennox Gastaut

A

Developmental delay
Multiple seizure type: absence, myoclonic, astatic and tonic
EEG = 1-2Hz spike and slow waves, polyspike bursts in sleep and slow background in wakefulness

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5
Q

medications acting on sodium channels are effective against

A

partial seizure

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6
Q

medications acting on T-type calcium channels are effective against

A

Absence seizure

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7
Q

In 1/3 of case, in patients developing febrile status epilepticus, what viral infection is MC assoc

A

HHV 6- HHV 7

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8
Q

TRIAD imaging findings in TB meningitis

A

Hydrocephalus
Basal Enhancements
Infarcts

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9
Q

CSF return to bloodstream within vacuoes in the process of

A

Pinocytosis

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10
Q

absolute C/I to LP

A

signs of inc ICP
local infection ate the desired puncture site
radiologic signs of obstructive hydrocephalus, cerebral
herniation and the presence of an intracranial mass lesion or midline shift

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11
Q

Relative C/I to LP

A

Signs of shock, sepsis or hypotension
Coagulation defect - DIC, platelet count <50,000/mm3, and warfarin use
Focal neurological deficit
GCS < 8
Epileptic seizures

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12
Q

test that differentiate viral and bacterial meningitis

A

Procalcitonin

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13
Q

DOC for Meningococcemia

A

Penicillin G 250,000-300,000 U/kg/day IV for 5-7 days
Ceftriaxone
Cefotaxime

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14
Q

Pen G allergy of Meningococcemia

A

Chloramphenicol
Ciprofloxacin
Meropenem

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15
Q

treatment for Status migrainosus (persistent HA lasting >3days)

A

Prochlorperazine IV 0.15mg/kg, max 10mg

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16
Q

Mutations in tuberous sclerosis

A

TSC1 encodes –> protein hamartin and TSC2 encodes –> protein tuberin.

17
Q

Diagnostic tests for GBS

A

CSF analysis: increased protein, normal glucose, no pleocytosis
Dissociation between high CSF protein and a lack of cellular response is diagnostic (albuminocytologic dissociation)

18
Q

Associated conditions with GBS

A

Cranial nerve deficits
Miller-Fisher syndrome: acute ophthalmoplegia, ataxia, areflexia

19
Q

MC malignant brain tumor in children

A

Medulloblastoma

at cerebellum
Homer wright rosette
4-8 y/o, M>F

20
Q

MCC of arterial ischemic stroke in pedia

A

Arteriopathy

21
Q

only drug may be used for benign infantile seizure

A

phenobarbital