Key result
Arrhythmogenic cardiomyopathy is a genetic disorder encompassing a spectrum of phenotypes, ranging from classical right ventricular to left ventricular forms.
Arrhythmogenic cardiomyopathy is recognized as a spectrum of phenotypes involving both the right and left ventricles, associated with high risks of arrhythmias and heart failure.
Arrhythmogenic cardiomyopathy (AC) is a genetic disorder characterized by high risk of life-threatening ventricular arrhythmias, sudden cardiac death, and progressive heart failure. Currently, there is evidence that AC includes a spectrum of cardiomyopathy phenotypes, ranging from the classical form of arrhythmogenic right ventricular cardiomyopathy (ARVC) to more recently identified forms of arrhythmogenic left ventricular cardiomyopathy.
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Mestroni et al. (2018) conducted a review in Arrhythmogenic cardiomyopathy. Arrhythmogenic cardiomyopathy is a genetic disorder encompassing a spectrum of phenotypes, ranging from classical right ventricular to left ventricular forms.
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