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Clinicopath Conf, Rapid-Onset-Dystonia-Parkinsonism Due to a Mutation in the ATP1A3 Gene
NEJM 362:2213-2219, Case 17-2010, 2010
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aphonia
Clinical Pathologic Conference(C.P.C.)
dysphagia
dystonia
dystonia,face
dystonia,focal
falling
gait disorder
gene mutation
hand weakness
hands,fisted
hemidystonia
imbalance,postural
movement disorder
movement disorder,extrapyramidal
MRI
MRI,negative
Parkinson disease,L-dopa nonresponsive
Parkinsonism syndrome
pull test
rapid onset dystonia parkinsonism
speech disorder
swallow evaluation
wide based gait
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