Pediatric Rehab Flashcards

1
Q

normal growth and developmental milestones - 6 months

A

manipulate objects and transfer across midline at 6 months
also generally suppression of reflexes at 6 months; broad generalization

using upper limb in more complex ways → this is when an upper extremity prosthesis might be first prescribed
left terminal radial limb deficiency (most common)

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2
Q

normal growth and developmental milestones - 1 year

A

walk at one
also age of rapprochment → child exploring close by then runs back to mother

“walk/wondering and one”

this is when a lower extremity prosthesis might be prescribed

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3
Q

primitive reflexes

A

typically (generalization) disappear by 6-8 months

moro: sudden startle when loss so support → infant outstretches arms
fencer: turning head → extension of limbs ipsilaterally, flexion contralaterally

palmar grasp: digits flex w stroking palm

babinski: toes up

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4
Q

normal growth and developmental milestones - 2 years

A

“two things”

2-word sentences
200 words
2/4 words are intelligible (50%)

starts to run (using two legs)

walks up stairs one foot at a time

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5
Q

normal growth and developmental milestones - 3 years

A

3-word sentences
¾ words intelligble (75%)
3 wheel bike

walks up stairs alternating feet

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6
Q

normal growth and developmental milestones - 4 years

A

more complex sentences and word choice
4/4 words intelligible

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7
Q

Malformations and TORCHS infections

A

variety of fetal malformations

toxoplasmosis
other (viruses)
rubella
CMV
herpes
syphilis

rubeolla not implicated in congenital malformations

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8
Q

genetic disorders

A

Down syndrome (trisomy 21): upward slanting eyes, simian crease, cardiac dz (endocardial cushion defects)

Turner syndrome (XO): webbed neck, shield chest, coarctation of aorta

Klinefelter syndrome (XXY): tall stature, gynecomastia, small testicles

all of these carry some degree of intellectual disability

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9
Q

congenital limb deficiencies - most common

A

left terminal radial deficiency

historically related to thalidomide exposure or maternal diabetes

prosthesis should enhance and not limit function (i.e., child never had a limb and prosthesis should not interfere with compensation/function)

Krukenberg procedure → separates radius/ulna → pincer grasp objects → sensation intact (unlike prostheses)

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10
Q

congenital limb deficiencies - most common LE

A

fibular hemimelia → leg length discrepancy → syme amputation

fibular is entirely absent (longitudinal deficiency)

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11
Q

congenital limb deficiency - partial proximal femoral focal deficiency (PFFD)

A

femur is short, patients also typically have a fibula deficiency

sometimes Van Ness Rotation → rotates short limb 180 degrees → intact foot can plantar/dorsi flex acting like the knee and can control new prosethesis

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12
Q

pediatric osseous defects - club foot

A

excessive severe equinovarus of foot, idiopathic →

plantar flexion, inversion, subtalar adduction → constantly rolling ankle w walking

Tx: PT, serial bracing (correct over time), surgery

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13
Q

pediatric osseous defects - tibia vara

A

abnormal varus bowing of proximal tibia d/t abnormal medial tibial growth plate

Tx: osteotomy of tibia

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14
Q

pediatric osseous defects - developmental hip dysplasia; Dx/PE, Tx

A

AKA congenital hip dislocation (bc easily dislocates)

malformation hip joint (femoroacetabular joint) → congenital dislocation of hip

Galleazzi: flex both knees with baby on back → knee is lower on dislocated hip side

Barlow: knees in flexion/adduction → posterior directed force dislocates hip

Ortolani: relocate hip and notice “clunk of relocation” by abducting thighs and applying anterior/medially directed force

US useful for Dx

Tx: Pavlik harness keeps femoral head in acetabulum for few months to prevent AVN

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15
Q

torticollis - pathophysiology, Px

A

intrauterine malpositioning → SCM scarring and excessive contraction → postural abnormality w head tilting towards affected SCM and chin turning away from affected SCM

Tx: PT, ROM of neck and SCM, surgery

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16
Q

grading of SCFE

A

head of femur slipping and sliding off femoral growth plate

Hx: obese adolescent male

PE: leg in external rotation

1: 0-33% sliding
2: 34-50% sliding
3: >50% sliding

Tx: always needs surgical pinning or else AVN

17
Q

Cobb angle for scoliosis

A

< 20 deg - observe
20-40 deg - Milwakee Brace 24 hours/day, very restrictive
> 40 deg - surgery

18
Q

Scheurmann dz

A

idiopathic juvenile kyphosis → restrictive lung pattern

XR: anterior kyphotic deformity, VB wedging, Schmorl nodes (nucleus pulposus leaks into adjacent vertebral body)

Tx: PT, TLSO brace, surgery

19
Q

Jones criteria, particularly migratory polyarthritis, and elevated CRP/ESR → Dx?

A

Hx Strep pyogenes (GAS) infection → systemic inflammatory reaction

Tx: PT, NSAIDs, steroids → reduce inflammation and maintain fucntion

20
Q

DMD - etiology, EDX

A

X linked recessive, Xp21 mutation → no dystrophin being produced → progressive myopathy w muscle tissue replaced by fibrosis starting w neck flexors

labs: elevated CK, muscle Bx shows fiber degeneration

NCS: normal SNAPs, CMAP amplitude low
EMG: myopathic motor units (SDSA, early recruitment, decreased insertional activity)

21
Q

myotonia congenita

A

genetic disorder → myotonia, spasms, muscle hypertrophy; worsed by cold weather → unable to smoothly grasp and release

NCS: normal
EMG: myotonic discharged (divebomber sound), otherwise normal

22
Q

juvenile rheumatoid arthritis - subtypes

A

polyarticular: many joints; worse prognosis if RF+ (majority RF-)

pauciarticular: <5 joints, but severe; usually ankles/knees; HLA B27+ and ANA+
* *ophthalmology referral** → mandatory bc risk of uveitis/iridocyclitis and needs regular slit lamps evals

systemic: multiorgan involvement + joints; fever/rash/hepatosplenomegaly

23
Q

CP subtypes and clinical presentation

A
spastic diplegia (paraplegia) most common
spasticity, scissoring, toe walking, crouch gait

dyskinetic - movement disorders
choreoathetosis, ataxia, dystonia

sitting up by age 2 = better prognosis for ambulating