Other neurological conditions Flashcards
cerebral palsy
neuromuscular disorder
spastic: hypertonia, hyperreflexia
dyskinetic: dystonia, athetosis, chorea
ataxic: cerebellum
monoplegia (one extremity), hemiplegia (half of body), paraplegia (both LEs), quadriplegia (all extremities), diplegia (greater LEs and some UEs)
complications: seizures, intellectual disabilities, contractures, language and cognitive deficits, dysarthria, visual impairments
ataxia
lack of coordination while performing voluntary movements
clumsiness, inaccuracy, instability
not smooth, jerky
chorea
brief, purposeless, involuntary movements of distal extremities and face
dyskinesias
involuntary, non repetitive, stereotyped movements
writhing
dystonia
abnormal postures and disruptions of ongoing movement
hemiballismus
flinging motions of the extremities
myoclonus
brief and rapid contraction of a muscle or group
tremors
rhythmic, alternating, oscillatory movements produced by repetitive patterns of muscle contraction and relaxation
parkinson’s
hypo kinetic CNS movement disorder
slowly progressive and degenerative pathways in basal ganglia (substantial nigra)
cardial signs: tremor, RIGIDITY, resistive motion, akinesia, festinating gait, falling
stage 1 - 5 (worst)
spina bifida
failure of the spinal column to fully form to protect the neural tube
occulta: bony malformation; may not discover until late childhood, red birthmark or patch of hair
cystica: exposed pich of SC and meninges
- with meningocele: protrusion of a sac through the spine with fluid and meninges, but not the spinal cord
- with myelomeningocele: protrusion of a sac through the spine with spinal cord/nerve roots
medical management of spina bifida
may not have many symptoms unless severe (such as tethered cord syndrome) and depending on what parts of the spine are involved
may change during growth spurts
during pregnancy, protect the sac from rupturing and from infections that could result in meningitis
shunt may be placed
increase in intracranial pressure
could cause intellectual disability
could result in Arnold chiari syndrome (portion of cerebellum and medula oblongata slip down into the foramen magnum to the cervical spinal cord)
if a shunt is blocked or infected (s/s are headache, vomiting, vision/mem problems, inc head size - medical emergency)
muscular dystrophies and atrophies
degenerative disorders resulting in mx weakness and decrease in mx mass
hereditary
due to absent mx protein - dystrophin and high creatine kinase
Duchenne’s muscular dystrophy
sex linked, recessive, males
enlarged calves
weakness in proximal joints
ambulating with a trendelenburg (waddling) gait, frequent falls
Gower’s sign - use hands to crawl up to thighs to get up off the floor
die around 20s
Becker’s muscular dystrophy
variant of duchennes
slower to progress, less severe, less predictable
survival can be in late adulthood if minimal cardiac involvement