Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is an inherited cardiomyopathy, usually transmitted with an autosomal dominant trait, characterized by right ventricular myocyte loss with fibrofatty replacement [1] . Clinical presentations in patients with ARVD/C vary widely. Heart failure, ventricular arrhythmias and sudden cardiac death (SCD) are the most severe clinical manifestations of ARVD/C.
Cardiovascular imaging in arrhythmogenic right ventricular dysplasia/cardiomyopathy
Inciardi, Riccardo M;Rossi, Andrea;Pesarini, Gabriele;Vassanelli, Corrado
2015-01-01
Abstract
Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is an inherited cardiomyopathy, usually transmitted with an autosomal dominant trait, characterized by right ventricular myocyte loss with fibrofatty replacement [1] . Clinical presentations in patients with ARVD/C vary widely. Heart failure, ventricular arrhythmias and sudden cardiac death (SCD) are the most severe clinical manifestations of ARVD/C.
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