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