Cardiac involvement in Emery-Dreifuss muscular dystrophy

Rainer Wessely, S. Seidl, A. Schömig

Research output: Contribution to journalArticlepeer-review

15 Scopus citations

Abstract

Emery-Dreifuss muscular dystrophy (EDMD) is a common form of muscular dystrophy frequently involving cardiac muscle, thus leading to dilated cardiomyopathy. Clinical outcome and prognosis is frequently determined by the involvement of the cardiac conduction system causing symptomatic bradyarrhythmias, as well as tachyarrhythmias and, if untreated, frequent sudden cardiac death. Typical features of the cardiac involvement of EDMD are presented, caused by a novel missense mutation in the splice receptor sequence of intron 6 of the LMNA gene on chromosome 1, encoding for the lamin A/C gene, consistent with the autosomal dominant form of EDMD.

Original languageEnglish
Pages (from-to)220-223
Number of pages4
JournalClinical Genetics
Volume67
Issue number3
DOIs
StatePublished - Mar 2005

Keywords

  • Cardiomyopathy
  • Conduction disease
  • Emery-Dreifuss
  • Lamin A/C
  • Muscular dystrophy
  • Mutation

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