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Published in 2020 at "Movement Disorders"
DOI: 10.1002/mds.28033
Abstract: Myoclonus‐dystonia (M‐D) is a rare hyperkinetic movement disorder characterized by upper body–predominant myoclonus and dystonia.1 A large proportion of cases are caused by autosomal‐dominant inherited mutations in the SGCE gene. In addition to the motor…
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Keywords:
motor;
natural course;
course myoclonus;
myoclonus dystonia ... See more keywords