| Literature DB >> 16534121 |
M C F Gerrits1, E M J Foncke, R de Haan, K Hedrich, Y L C van de Leemput, F Baas, L J Ozelius, J D Speelman, C Klein, M A J Tijssen.
Abstract
The epsilon-sarcoglycan (SGCE) gene is an important cause of myoclonus-dystonia (M-D), although the majority of cases with an M-D phenotype test negative. Seven of 31 patients with the M-D phenotype carried a mutation in the SGCE gene. Positive family history and truncal myoclonus were independent prognostic factors. Early disease onset, onset with both myoclonus and dystonia, and axial dystonia were detected significantly more often in the mutation carriers.Entities:
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Year: 2006 PMID: 16534121 DOI: 10.1212/01.wnl.0000201192.66467.a3
Source DB: PubMed Journal: Neurology ISSN: 0028-3878 Impact factor: 9.910