Neurological System Disorders (Ch7) Flashcards
Stage of Parkinson’s: confined to wheelchair or bed, maximally assisted
Stage V
myelinated nerve fibers located centrally
white matter
paralysis of the upper brachial plexus, resulting in the “waiter’s tip” position
Erb’s palsy
which cerebral hemisphere does this? emotion
right
contain cell bodies that give rise to efferent (motor) neurons
anterior horns
manifested by loss of voluntary, but preservation of reflexive eye movements, bradykinesia, rigidity, axial dystonia, pseudobulbar palsy, and dementia
progressive supranuclear palsy
which cerebral hemisphere does this? visual reception from right field
left
acute, rapidly progressive form of polyneuropathy characterized by symmetric muscular weakness and mild distal sensory loss; onset of recovery is 2-4 weeks after 1st symptoms; may be accompanied by respiratory failure and dysphagia
Guillain-Barre Syndrome
MACS Level: handles objects easily and successfully
I
MACS Level: does not handle objects and has severely limited ability to perform even simple actions
V
GMFCS Level: walks with assistive mobility devices; limitations walking outdoors and in the community
III
tracts that are important for voluntary motor control
corticospinal tracts
contain afferent (sensory) neurons
posterior horns
masses of gray matter deep within the cerebral hemispheres; involved in motor planning
basal ganglia
which cerebral hemisphere does this? visual spatial processing
right
MACS Level: handles objects with difficulty; needs help to prepare and/or modify activities
III
variant of Duchenne muscular dystrophy that is slower to progress, less severe, and less predictable
Becker muscular dystrophy
how many thoracic vertebra are there?
12
if a patient with spina bifida presents with enlarged head, severe headache, vomiting, and/or irritability, what does this indicate?
shunt malfunction
which cerebral hemisphere does this? interpretation of abstract information
right
type of muscular dystrophy that involves the face, upper arms, and scapular region, causing masking, weakness, decreased facial mobility, and inability to lift arms above shoulder level; progresses slowly and rarely affects life expectancy
fascioscapulohumeral muscular dystrophy
a hypokinetic CNS movement disorder that is idiopathic, slowly progressive, and degenerative; begins with a resting “pill-rolling” tremor of one hand
parkinson’s disease
Presence of weakness, deformities, and associated joint contractures; position of rest for the UE tends to be IR of the shoulders, elbow extension, wrist flexion, hip flexion and IR, clubfeet
Arthrogryposis multiplex congenita
a lesion of the motor cortex will result in spasticity with flexor and extensor imbalance, which can be expressed as hypertonia or hyperreflexia
spastic cerebral palsy