MS part 1 Flashcards

1
Q

down syndrome

A

overexpression of genes found on chromosome 21

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2
Q

what do pt’s eventually develop with down syndrome

A

alzheimers

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3
Q

what is treatment directed towards with down syndrome

A

medical problems presented

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4
Q

common problems with older down syndrome pt’s

A

obesity
DM
CV
osteoarthrititic degenration of the spine - nerve pain
osteoporosis of vertebral or long bone fx

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5
Q

clinical manifestations with down syndrome

A
  • muscle hypotonia
  • atlantoaxial instability secondary to ligamentous laxity
  • feeding disorders
  • cardiac defects
  • flat occiput
  • recurrent patellar dislocations
  • excessive foot pronation
  • late hip dislocations
  • scoliosis
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6
Q

scoliosis

A
  • abnormal lateral curvature of spine
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7
Q

what can scoliosis cause

A
  • limb length inequality
  • muscular dystrophy
  • rotation of vertebral column around its axis occurs and causes associated rib cage deformity –> restrictive lung disease
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8
Q

functional scoliosis

A
  • postural defect secondary to pain, poor posture, leg length discrepancy & muscles spasms
  • can be corrected
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9
Q

structural scoliosis

A
  • fixed curvature of the spine associated with vertebral rotation and asymmetry of the ligamentous supporting structures
  • congenital
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10
Q

if the curvature of scoliosis is <20 deg, what can occur?

A

rarely causes problems

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11
Q

if curvature for scoliosis is >60 degrees, what can happen

A
  • severe issues
  • pulmonary insufficiency
  • reduced lung capacity
  • back pain
  • degenerative spinal arthritis
  • disk disease
  • sciatica
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12
Q

management of scoliosis for PT

A
  • prevention of postural scoliosis

- exercises and ESTIM for pt with muscular imbalances

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13
Q

PT management for scoliosis

A
  • exercise for paraspinals

- strengthen trunk extensors, abs, gluteal muscles, iliopsoas & hip extensors

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14
Q

prognosis for scoliosis

A

depends on likelihood of progression

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15
Q

curvature <40 at skeletal maturity

A

progression small

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16
Q

curvature >50 at skeletal maturity

A
  • spina biomechanically unstable

- curve likely to progess throughout life

17
Q

spinda bifida

A
  • occur when the neural tube doesn’t properly close during embryo phase
  • incomplete fusion of the posterior vertebral arch (meninges do not protrude)
18
Q

meningocele

A
  • external protrusion of meninges
  • forced into gaps within vertebrae
  • minor disabilities, no nerve damage
19
Q

myelomeningocele

A
  • most severe

- protrusion of the meninges and SC

20
Q

hydrocephalus

A
  • build up of too much CSF in the brain

- treatment: shunting

21
Q

are mental functions compromised in pt’s with hydrocephalus

A

no

22
Q

developmental dysplasia of the hip (DDH)

A
  • ball of the femur is loose in the socket and be easy to dislocate - can lead to ligamentous laxity
  • socket too shallow or not there
23
Q

treatment for DDH

A

encourage ROM but avoid displacement of the hip

24
Q

muscular dystrophy

A

ongoing, symmetric, muscle loss/weakness with increasing deformity and disability

25
Q

duchenne’s MD

A

most common
alterations of protein dystrophin
repeated bouts of muscle damage lead to atrophy & fibrosis, eventually muscle degeneration

26
Q

when is MD identified in children

A

when the child has difficulty getting up off the floor, falls frequently, difficulty climbing stairs, waddling gait, increased lumbar lordosis

27
Q

what gait pattern is often seen with MD

A

tredelenburg

ambulation continues to deteriorate

28
Q

shoulder involvement seen with MD

A

scapular winging

instability

29
Q

other things seen with MD

A
scoliosis
cognitive loss
respiratory restrictive disease
cardiac, dilated cardia myopathy
GI
30
Q

prognosis for MD

A

pulmonary and cardiac complications bring down prognosis

31
Q

interventions for MD

A

active as possible
dont over exercise
aquatic therapy
diaphragmatic breathing

32
Q

osteogenesis imperfecta (OI)

A

brittle bone disease

disease of collagen synthesis affecting bones and CT

33
Q

OI management

A

fx prevention and control

splints

34
Q

torticollis

A
  • dystonia
  • syndrome of involuntary sustained or spasmodic muscle contractions involving co-contractions of the agonist and antagonist
  • contracted SCM
  • not a diagnosis
35
Q

which way does the head tilt with torticoliis

A

contracted SCM produces head tilt to the affected side with rotation of chin to opposite side

36
Q

PT implications for torticollis

A

stretch and strengthen neck muscles