Abstract
Arrhythmogenic cardiomyopathy (ACM) is a genetic cardiomyopathy which is characterized by progressive fibro-fatty replacement of the myocardium. Clinically, this disease may lead to life-threatening arrhythmias and heart failure. Since ACM is an inherited cardiomyopathy, the relatives of ACM patients are also at a certain risk of developing this disease. However,
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