Pediatric Neurology Flashcards

1
Q

a. Fasciculation’s absent

A

UMN

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2
Q

gait unsteady until age

A

6

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3
Q

babinski goes down after

A

18 months

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4
Q

most reflexes are integrated by what month

A

6 moths

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5
Q

what is the most concerning HA pattern

A

chronic, progressive

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6
Q

chronic and progressive HA think what

A

increased ICP

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7
Q

increased ICP HA is worse when what

A

they lie flat

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8
Q
  1. Frontal, bitemporal or unilateral pounding/throbbing for 2-72h
A

migraines

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9
Q

what is the first treatment for migranes

A

eliminate triggers

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10
Q

what is the pharm treatment for migranes

A

NSAID,
acetaminophen,
Triptans

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11
Q

AKA idiopathic intracranial hypertension

A

Pseudotumor Cerebri

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12
Q

a. Increased ICP without space occupying lesion

A

Pseudotumor Cerebri

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13
Q

a. Most common in children of childbearing age can happen in kids > 11

A

Pseudotumor Cerebri

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14
Q

a. Papilledema on PE

A

Pseudotumor Cerebri

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15
Q

, vision loss often chief complainant

A

Pseudotumor Cerebri

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16
Q

what is the MC type of CP

A

1.spastic

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17
Q

4 types of CP

A

spastic
athetoid
ataxic
atonic

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18
Q

a. Neural tube disorder (NTD) = defective closure of the caudal neural tube early in gestation (about week 4)

A
  1. Spina Bifida
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19
Q
  1. Spina Bifida

types 3

A

i. Myelomeningocele
i. Meningocele
i. Spina bifida occulta

20
Q

how do you prevent spina bifida

A

folic acid

21
Q

DX of spina bifida 2

A
  1. alpha-fetoprotein (AFP) level (16-18 weeks

2. US 20 weeks

22
Q

i. Hypopleasia

associated with what chiari

23
Q

i. Herniation below the formen magnum

24
Q

i. Hydrocephalus

ii. Myelomeningocele

25
i. Sx related to ventricular distention and increased ICP due to obstruction of CSF flow
Hydrocephalus
26
Headache, vomiting, altered mental status, visual changes, ocular nerve palsies, and focal neurologic findings
Hydrocephalus
27
a. Progressive degeneration of the anterior horn cells progressive weakness of lower motor neurons b. Genetic (autosomal recessive) c. Presents with progressive proximal weakness , decreased spontaneous mvmt, “floppiness” d. Normal mental, social and language skills. Sensation is preserved. e. Decreased facial expression and drooling f. Dx: EMG, muscle bx, DNA testing
SMA
28
Campylobacter jejuni
GBS
29
i. Ascending weakness (symmetric) ii. May have autonomic nerve dysfunction iii. Children- refusal to walk and leg pain are most common presenting symptoms
GBS
30
i. LP- elevated CSF protein without increased WBC
GBS
31
treatment for GBS
IVIG | plasmaphoresis
32
a. Gower’s sign b. Proximal muscles affected first, then distal; lower first, then upper - calf hypertrophy
1. Duchenne Muscular Dystrophy
33
muscle that is X liked recessive
1. Duchenne Muscular Dystrophy
34
1. Diagnosis a. Serum CK b. biopsy c. genetic testing
DMD
35
a. more common, autosomal dominant (chromosome 17)
NF: 1
36
- also autosomal dominant (chromosome 22)
NF 2
37
i. Referred to as peripheral type | ii. More skin and brain abnormalities
NF: 1
38
i. Manifests as bilateral vestibular schwannomas (VIII nerve tumors)
NF: 2
39
Café-au-lait spots are NOT part of NF type 2
TRUTH
40
Most common neurologic disorder of infants & young children
Febrile Seizure
41
what age can you have febrile seizure
6 - 5 years
42
a. Viral infections commonly associated (HHV-6, influenza)
1. Febrile Seizure
43
a. Low-risk for long term neurologic complications
1. Febrile Seizure
44
a. IV benzos
for Sz lasting longer than 5 minutes
45
a. Brain & skin have same embryonic origin
Truth