Neuro/MSK Flashcards

1
Q

HIE

  • primary energy failure?
  • secondary energy failure?
A
  • primary energy failure: immediate necrotic cell death from decreased phosphocreatine and ATP - infant may be able to recover
  • secondary energy failure (6-48 hours): glutamate (excitatory) release –> calcium influx into cells –> free radicals –> caspases –> apoptosis

Goal of TH is to reduce apoptosis

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2
Q

Whats parts of the brain are affected in:

  • HIE
  • metabolic disorders
  • kernicterus
A
  • PLIC
  • PLIC
  • basal ganglia, globus pallidus, and cerebellum
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3
Q

Dandy Walker

A

posterior fossa cyst and cerebellar hypoplasia, 4th ventricle enlargement

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4
Q

Treatment of SIADH, central DI, and nephrogenic DI

A

SIADH: too much ADH
– fluid restriction, lasix if needed
Central: ADH not produced
– DDAVP
Nephrogenic: ADH produced but kidneys can’t respond
– Thiazides (paradoxical effect; increases prox reabsorption of Na and water)

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5
Q

If you see term infant with IVH or thalamic hemorrhage, what should you think of?

A

cerebral sinovenous thrombosis - get MRI

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6
Q

What do periodic lateralized epileptiform discharges suggest?

A

HSV or stroke

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7
Q

What electrolyte abnormality do infants with holoprosencephaly have?

A

hypernatremia (central DI from abnormal hypothalamus which sets an abnormal osmostat; pituitary is actually fine)

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8
Q

What nerve roots are affected in:

  • Erb’s palsy
  • Waiter’s tip
  • Klumpke’s
  • Horner’s
A
  • Erb’s palsy (grasp present, biceps absent) - C5-6
  • Waiter’s tip (grasp present) - C7
  • Klumpke’s (grasp absent) - C8-T1
  • Horner’s (ptosis, miosis, anhydrosis) -
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9
Q

Most common cranial nerve injury during birth?

A

facial nerve (asymmetric cry, can’t close eye on that side) - give eye drops and tape eyelid

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10
Q

Which craniosynostosis repair is for cosmetic reasons? Which is for brain growth?

A

sagittal for cosmetic reasons

coronal (or if multiple sutures) for neurodevelopment

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11
Q

Brain tumors in neonate…

  • most common type?
  • supratentorial or infratentorial?
  • common presentation?
A
  • teratoma
  • supratentorial
  • bulging fontantelle or macrocephaly
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12
Q

Fingers:

  • hyperconvex fingernails and polydactyly?
  • hypoplastic fingernails and overlapping fingers?
  • shortened fourth finger?
  • clinodactyly of fifth finger?
  • 3,4 syndactyly?
A
  • hyperconvex fingernails and polydactyly: T13
  • hypoplastic fingernails and overlapping fingers: T18
  • shortened 4th finger: Turners
  • clinodactyly: Downs
  • 3,4 syndactyly: triploidy
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13
Q

diurnal variation in CP-like symptoms?

A

Dopa-responsive dystonia - treat with small doses of dopamine

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14
Q
  • Primary neurulation problems?
  • Secondary neurulation problems?
  • Ventral induction?
  • Neural migration?
  • Organization?
  • Myelination?
A
  • Primary neurulation - myelomeningocele, arnold-Chiari
  • Secondary neurulation - Spinal problems
  • Ventral induction - Agenesis of corpus collosum
  • Neural migration - lissencephaly, schizencephaly, pachygyria
  • Organization - T21, autism
  • Myelination - prematurity, malnutrition
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15
Q

Do hearing tests detect high or low frequency hearing loss better?

A

Better at detecting high frequency hearing loss better

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16
Q

Levels of lesion of myelomeningocele and ambulation potential?

A
  • cervical, thoracic, and thoracolumbar (C1-L2): no reflexes, poor ambulation potential
  • lumbar (L3-L4): knee jerk, ambulate with crutch
  • lumbosacral (L5-S1): ankle jerk, ambulate w/ or w/o crutch
  • sacral (S2-S4): anal wink, ambulate well
17
Q

Reflexes?

A

26 - palmar, blinking
28 - rooting, moro
30 - crossed extensor, gallant
34 - pupillary constriction, tonic neck, placing and stepping

“peanut butter rules my every go”

18
Q

SMA has some normal things…(4)

A
  • normal extraocular movements
  • normal diaphragmatic function
  • normal sphincter function
  • normal sensory exam
19
Q

proximal limb weakness upper>lower =

A

parasagittal cerebral injury

20
Q

what finding predicts spastic diplegia lower > upper

A

PVL

21
Q

what biomarkers correlate with mod-severe HIE?

A

elevated: S100 beta, IL-6, GFAP, neuron-specific enolase, and brain-derived neurotrophic factor

22
Q

Which OI type is most likely to be seen in NICU? symptoms?

A

Type 3 - triangular facies, rib fractures, short, hyperlaxity

Type 1 is least severe, type 2 dies in utero, 4 and 5 are moderately severe

1 you win, 2 is boo, 3 is free from death for now

23
Q

high CPK in what three things?

A

MCAD, Pompe’s, muscular dystrophy

24
Q

The primary cellular target in PVL is?

A

oligodendrocyte progenitors