| Literature DB >> 15623712 |
B G H Schoser1, K Ricker, C Schneider-Gold, C Hengstenberg, J Dürre, B Bültmann, W Kress, J W Day, L P W Ranum.
Abstract
Medical records and follow-up data were reviewed in 297 genetically proven myotonic dystrophy type 2 (DM2) patients. Patients were selected by the criteria of cardiac sudden death before age 45. Sudden death occurred in four patients, three of whom were cardiological asymptomatic, and one with a history of heart failure. Cardiac histopathology showed dilated cardiomyopathy in all, and conduction system fibrosis in two patients. Pathogenetic CCUG ribonuclear inclusions were demonstrable in cardiomyocytes.Entities:
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Year: 2004 PMID: 15623712 DOI: 10.1212/01.wnl.0000147335.10783.e4
Source DB: PubMed Journal: Neurology ISSN: 0028-3878 Impact factor: 9.910