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torticollis
SCM affected: flexion, ipsilateral SB, contralateral rotation
plagiocephaly
prolonged positioning creating P on skull โ ipsilateral occipital flattening and contralateral bulging
tendency to lie on one side flattens skull and shifts it forward
helmet: worn 20 - 23 hours per day for 2 - 7 months (no longer useful at 18 months)
cerebral palsy
nonprogressive encephalopathy
CP birth
preterm
CP primary causes
hemorrhage under ventricles, hypoxic encephalopathy, malformation, or trauma of CNS
spasticity
velocity dependent
increased tone
lesion of motor cortex
LE muscles affected: hip flexors, adductors, IRs, knee flexors, ankle PFs
UE muscles affected: scapular retractors, shoudler extensors and adductors, elbow flexors, forearm pronators
spastic CP gait
crouched gait or toe walkers
dystonia
involuntary movements with sustained contracitons
hypertonic: PROM stiffness
ataxia
coordination or timing disorder
lesion of cerebellum; instability of movement
low tone
wide BOS
intention tremors
nystagmus
athetoid
slow writhing movements (wormlike; involuntary
fluctuating muscle tone
normally decreased muscle tone (floppy baby syndrome)
distal UE commonly involved
level 1 GMFCS for CP
walk without restriction, limitations in advanced gross motor skills
level 2 GMFCS for CP
walk without AD, limitations walking outdoors and in the community
level 3 GMFCS for CP
walk with AD, limitations walking outdoors and in the community
level 4 GMFCS for CP
self-mobility limited, power mobility outdoors and in the community
level 5 GMFCS for CP
self-mobility severely limited even with assistance, may use standing frame for WB, WC bound
spina bifida
neural tube defect resulting in vertebral and/or SC malformation
hydrocephalus signficantly related to closure of neural tube defect
SB myelomeningocele
CSF, SC tissue, and nerve fibers
SB meningocele
cyst includes CSF but SC is intact
spina bifida occulta
closed lesion; no SC involvement
atypical skin pigmentation, large dimple, or tuft of hair
common impairments with SB
kyphoscoliosis, shortened hip flexors and adductors, flexed knees, pronated feet
tethered cord syndrome: spasticity, increased tone, buttocks pain, increased scoliosis, weakened leg muscles
sensory loss
L4 - 5 lesions
cognitive impairments
club foot
bowel and bladder dysfunction
latex allergy
arthrogryposis
nonprogressive condition
multiple joint contractures and muscle weakness throughout body at birth
autism
developmental disorder that appears within first 3 years of life
impairments
social communication skills
sensory processing issues
repetitive behaviors
dyspraxia: inability to imitate movement; disconnect between idea of movement and motor execution
decreased coordination
balance impairments
hypotonia
down syndrome
extra copy of 21st chromosome
impairments
hypotonia, ligament laxity
delayed motor milestones
deficits in memory and expressive language
congenital heart defects
impairments of postural control and coordinaiton
decreased strength of quads and hip abductors
red flag with down syndrome
atlantoaxial instability
s/s atlantoaxial instability
decreased strength and ROM, hyporeflexive, decreased sensation in extremities, persistent head tilt
duchenne muscular dystrophy
X-linked recessive, inherited disorder
dystrophin gene missing
impairments
pseudohypertrophic calves
progressive weakness
delayed walking
frequent falls
difficulty rising from supine or sitting
gowers sign
cardiac tissue affected
decreased respiratory function
contractures and deformities
what is important to avoid in patients with DMD
maximal exercise - damages muscles
brachial plexus injury
traction or compression injury to unilateral brachial plexus during birth process or cervical rib abnormality
erb palsy
C5 - 6
shoulder adducted and IR, elbow ext, forearm pronated, wrist flexed (waiterโs tip)
klumpke palsy
C8 - T1
intrinsic muscles of hand and wrist, wrist ext, fingers flexed (claw hand)