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SY11.3 Clinical Neurophysiological Assessment of Myoclonus

✍ Scribed by Mark Hallett

Book ID
119607558
Publisher
Elsevier Science
Year
2009
Tongue
English
Weight
46 KB
Volume
120
Category
Article
ISSN
1388-2457

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## Abstract Mutations in the ϡ‐sarcoglycan (__SGCE__) gene have been associated with DYT11 myoclonus‐dystonia syndrome (MDS). The aim of this study was to characterize myoclonus in 9 patients with DYT11‐MDS presenting with predominant myoclonus and mild dystonia by means of neurophysiological techn

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Myoclonus can be diagnosed and classified mainly based on clinical features. Neurophysiologic studies help confirm clinical diagnosis and classification, and understand underlying physiological mechanisms. The neurophysiologic classification of myoclonus is mainly based on surface EMG (individual EM