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Article

Arrhythmogenic right ventricular cardiomyopathy/dysplasia: a review and update.

Clinical research in cardiology : official journal of the German Cardiac Society - 1 May 2011

Azaouagh A, Churzidse S, Konorza T, Erbel R

Abstract excerpt

Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is a predominantly genetically determined and heritable form of cardiomyopathy that is characterized pathologically by the replacement of myocytes by adipose and fibrous tissue and leads to right ventricular failure, arrhythmias, and sudden cardiac death. The estimated prevalence of ARVC/D in the general population ranges from 1 in 2,000 to 1 in...

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PMID: 21360243
DOI: 10.1007/s00392-011-0295-2

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DSP
JUP

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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