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

doi:10.1007/s00392-011-0295-2

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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...

Topics

Arrhythmogenic Right Ventricular Dysplasia
Female
Genetic Predisposition to Disease
Heart Function Tests
Heredity
Humans
Male
Patient Selection
Predictive Value of Tests
Risk Assessment
Risk Factors
Treatment Outcome

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Open in PubMed

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

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