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Myoclonus‐dystonia: An update
Author(s) -
Kinugawa Kiyoka,
Vidailhet Marie,
Clot Fabienne,
Apartis Emmanuelle,
Grabli David,
Roze Emmanuel
Publication year - 2009
Publication title -
movement disorders
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.352
H-Index - 198
eISSN - 1531-8257
pISSN - 0885-3185
DOI - 10.1002/mds.22425
Subject(s) - myoclonus , dystonia , neuroscience , movement disorders , neurological disorder , neurophysiology , medicine , physical medicine and rehabilitation , psychology , central nervous system disease , pathology , disease
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 recommendationsfor clinical management. © 2008 Movement Disorder Society