Pedia Hx and PE Flashcards

1
Q

age when adult neuro exam can be used in children

A

4 yo

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2
Q

most useful and objective information

A

observation at play

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3
Q

traits making children more predisposed to injury

A

top heavy
cranial bones are thin and not well developed
brain is highly vascular
excessive spinal mobility
wedge shaped cartilaginous vertebral bodies

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4
Q

characteristics of sturge weber syndrome

A

port wine stain

vascular malformations in the brain –> calcification and sequelae of epilepsy and developmental delay

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5
Q

characteristics of neurofibromatosis

A

cafe au lait sport
axillary freckling
neurofibromas
neruologicaldeficits

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6
Q

characteristics of ataxia telangiectasia

A

telangiectatic lesions in conjunctiva, skin, mucosa
progressive cerebella ataxia
can be misdiagnosed as ataxic cerebral palsy

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7
Q

characteristics of neurocutaneous melanosis

A

seizures most common presentation

partches of hyperpigmentation and tufts of hair

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8
Q

when to measure head size

A

babies to 3 yo

>3 yo with small head size

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9
Q

early closure of cranial sutures

A

primary craniosynostosis
>/= 1 sutures fuse prematurely = restricted perpendicular skull growth
multiple sutures = inc icp

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10
Q

early fusion of sagittal suture

A

scaphocephaly

long and narrow head

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11
Q

early fusion of one coronal suture

A

anterior plagiocephaly
asymmetrical head
“harlequin” deformity

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12
Q

early bilateral coronal suture fusion

A

brachycephaly

short head but wide, cone shape

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13
Q

early closure of one lambdoid suture

A

posterior plagiocephaly

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14
Q

early fusion of the metopic suture

A

trigonocephaly

triangle shaped forehead

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15
Q

features of trisomy 21

A
protruding tongue
flat nasal bridge
epicanthal folds
single palmar crease
congenital cardiac defect
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16
Q

features of gargoylism

A

gapped teeth
thickened tongue
frontal bossing
associated with hunter’s syndrome

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17
Q

features of tunrner syndrome

A

mental retardation
webbed neck
heart shaped face
low hairline at back

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18
Q

features of prader willi syndrome

A

almond eyes
downturned mouth
hypogonadism

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19
Q

features of treacher-collins syndrome

A

underdevelopment of jaw and zygomatic bones
precursors of ear fail to develop
cc: deafness

20
Q

how to measure occipitofrontal circumference

A

most prominent part of glabella around most prominent part of the occiput
during first 2 months and then 2x a year after

21
Q

normal head circumference and growth

A

table 4

22
Q

normal hc vs cc

A

hc > cc at birth
hc = cc at 6 mos
hc < cc at end of 1st year

23
Q

what are craniotabes

A

softening of parietal or occipital bones

indicates prematurity or rickets

24
Q

closure of anterior fontanelle

A

earliest: 8 mos
latest: 17-19 mos

25
Q

closure of posterior fontanelle

A

6-8 weeks

26
Q

t/f in younger children whose sutures have not yet mineralized increased icp may result with a child with a bigger head

A

true

12 yo: vomiting and increased sensorium

27
Q

normal transillumination of the skull

A

2 cm halo of light in frontoparietal

1 cm halo of light in occipital

28
Q

abnormal transillumination of the skull

A

uniform transillumination = thinned or absent cortex
(+) setting sun sign = hydrocephaly
decreased area of transillumination = subdural hematoma

29
Q

what to look out for in palpation of the spine

A

sacrum and coccyx present (sacral agenesis)
spina bifida occulta (hairy or pigmented patch over lower spine)
sacrococcygeal pit

30
Q

when is babies eyesight 20/20

A

6 mos

31
Q

when can visual acuity be tested

A

> 4 yo

32
Q

how to test visual field

A

toys to get attention

33
Q

how to test oculomotor system

A

doll’s eye maneuver

toys

34
Q

how to test cn 7

A

smiling and crying

35
Q

when can infants localize sound

A

6 mos

36
Q

t/f muscle fasciculations & atrophy are best demonstrated in tongue

A

true

37
Q

tremors at rest signal __

A

cns disease

38
Q

signs of hypotonic infant

A

supine: frog leg posture
suspended in prone: limbs and head hang limply like rag doll
resting posture: extended elbows, hips, and knees (should be flexed)

39
Q

when does hypertonia decrease

A

after 3 mos

40
Q

what is gowers sign

A

pushing up unto one’s legs otherwise being unable to rise

41
Q

characteristics of tetanus

A

acute onset hypertonia, painful muscular contractions

generalized muscle spasms

42
Q

spasticity vs rigidity

A

spasticity: umn, clasp-knife phenomenon
rigidity: extrapyramidal, cogwheel rigitiy

43
Q

most reliable reflexes

A

biceps, knee, and ankle jerk

44
Q

normal clonus in childdren

A

< 3 mo: 5-10 beats

older children: 1-2 beats

45
Q

primitive reflexes

A

moro reflex (falling head)
grasp reflex
asymmetric tonic neck reflex (fencing)
parachute reflex (falling trunk)