Abstract
A few cases of familial occurrence of arrhythmogenic right ventricular (RV) disease have been reported. 1–5 The afflicted persons were almost always men. In most cases the underlying condition was RV dysplasia, i.e., a pathomorphologic entity characterized by abnormal development of part of the RV wall. 1 We describe a family consisting of 4 siblings, of whom 1 of 3 brothers and a sister had recurrent ventricular arrhythmias.
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