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Myoclonus-Dystonia: An Update

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MOVEMENT DISORDERS
卷 24, 期 4, 页码 479-489

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WILEY
DOI: 10.1002/mds.22425

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myoclonus-dystonia; primary dystonia; clinical neurology; epsilon-sarcoglycan; genetics; pathophysiology

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Our knowledge of the clinical, neurophysiological, and genetic aspects of myoclonus-dystonia (M-D) has improved markedly in the recent years. Basic research has provided new insights into the complex dysfunctions involved in the pathogenesis of M-D. On the basis, of a comprehensive literature search, this review summarizes current knowledge on M-D, with a focus on recent findings. We also propose modified diagnostic criteria and recommendations for clinical management. (C) 2008 Movement Disorder Society

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