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Article

Mechanisms of disease: molecular genetics of arrhythmogenic right ventricular dysplasia/cardiomyopathy.

Nature clinical practice. Cardiovascular medicine - 1 May 2008

Awad Mark M, Calkins Hugh, Judge Daniel P

Abstract excerpt

Arrhythmogenic right ventricular dysplasia/cardiomyopathy is an inherited cardiomyopathy estimated to affect approximately 1 in 5,000 individuals. Cardinal manifestations include right ventricular enlargement and dysfunction, fibrofatty replacement of myocytes in the right ventricle, characteristic electrocardiographic abnormalities, and ventricular arrhythmia most commonly arising from the right ventricle. The...

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PMID: 18382419
DOI: 10.1038/ncpcardio1182
PMCID: PMC2822988

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