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33 Cards in this Set

  • Front
  • Back
sign that is often present immediately following stroke
babinski
unidirectional increase in muscular tone
spasticity (UMN lesion)
bidirectional increase in tone to passive range of motion
rigidity (UMN lesion)
bidirectional resistance to passive motion that increases w/ force and rate of movement
paratonia (UMN lesion)
deletion of chromosome 4
facioscapulohumeral md
CTG trinucleotide repeat in chromosome 19
myotonic dystrophy
trinucleotide repeat of myotonic dystrophy
CTG
muscular dystrophy with more distal involvement of muscles
myotonic dystrophy
fatiguing weakness followed by rest and recovery
myasthenia gravis
drug used to dx myasthenia gravis
edrophonium
drug used to tx myasthenia gravis
pyridostigmine
areas of sensory loss do not match up with territories of individual n.
polyneuropathy
stocking glove weakness is an example of what kind of neuropathy
polyneuropathy
UMN + LMN
ALS
motorneuron disease where DTRs are absent
werdnig-hoffman (seen in infants)
numbness is present in what group of neuromuscular disease
polyneuropathy
group of neuromuscular disease with high CK
myopathy
NM group with more proximal weakness than distal
myopathy (except myotonic dystrophy)
myasthenia gravis
NM group with more distal weakness than proximal
polyneuropathy
motoneuron disease (except kugelberg-weilander)
NM group with fatiguing weakness
myasthenia gravis
NM group with reduced or absent DTR
polyneuropathy
(motoneuron - only werdnig)
motoneuron disease with absent DTR
werdnig-hoffman (infants)
NM group with fasciculations
motoneuron
NM group with numbness
polyneuropathy
NM group with large increase in CK
myopathy
NM group with decreased nerve conduction velocity
polyneuropathy
bilaterally symmetric sensory/motor loss
polyneuropathy
causes of polyneuropathies
DM
alcohol
motoneuron disease
progressive bulbar palsy (brainstem)
ALS (UMN + LMN)
spinal muscular atrophy (LMN)
-werdnig (infants)
-kugelberg
two types of myopathies
genetic: muscular dystrophy
acquired: polymyositis, dermatomyositis
protein deficient in duchenne
dystrophin
muscular dystrophy that affects the face, and shoulder area
facioscapulohumeral md
tumor that is assx with myasthenia gravis
thymoma