4.5 Article

Treatment of myoclonus-dystonia syndrome with tetrabenazine

Journal

PARKINSONISM & RELATED DISORDERS
Volume 20, Issue 12, Pages 1423-1426

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.parkreldis.2014.09.029

Keywords

Myoclonus; Dystonia; Tetrabenazine; Blinded; Dopamine

Funding

  1. National Institutes of Health [RO1 NS069936, RO1 NS082296, U54 NS065701, RO1 NS040470, RO1 HD053312]
  2. Bachmann-Strauss Dystonia & Parkinson Foundation
  3. Benign Essential Blepharospasm Research Foundation
  4. Dystonia Medical Research Foundation
  5. Tyler's Hope for a Cure

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Background: Many cases of myoclonus-dystonia (M-D) are due to mutations in SGCE (DYT11). For the majority of patients, myoclonus is relatively more severe than dystonia and can lead to significant functional disability. Deep brain stimulation has been chosen as a treatment option in some patients given that M-D often responds poorly to oral pharmacotherapy. Methods: Two siblings with M-D due to the same SGCE deletion mutation were evaluated with the Global Dystonia Rating Scale (GDRS), Fahn-Marsden Rating Scale (FM) and Unified Myoclonus Rating Scale (UMRS) on and off tetrabenazine. Results: Both subjects showed marked improvement in myoclonus and mild-to-moderate improvement in dystonia with tetrabenazine. In addition, the response to tetrabenazine has been sustained for years. Conclusions: A therapeutic trial of tetrabenazine should be considered in patients with M-D, especially before consideration of deep brain stimulation. An adequately powered multi-center, double-blind study of tetrabenazine will be required to determine the relative contributions of tetrabenazine therapy to myoclonus, dystonia, quality of life, and activities of daily living in patients with M-D. (C) 2014 Elsevier Ltd. All rights reserved.

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