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We sought to investigate the clinical-genetic profile of left-dominant arrhythmogenic cardiomyopathy (LDAC).In the absence of coronary disease and left ventricular (LV) systolic dysfunction, lateral T-wave inversion and arrhythmia of LV origin are often considered benign. Similarly, chest pain with enzyme release might be attributed to viral myocarditis. We hypothesized that these abnormalities might...
Primary cardiomyopathies are heart muscle diseases intrinsic to the myocardium. This group includes dilated cardiomyopathy (DCM), arrhythmogenic cardiomyopathy (ARVC), hypertrophic cardiomyopathy (HCM), restrictive cardiomyopathy (RCM) and unclassified cardiomyopathy. The cardiomyopathies may be classified pathophysiologically and display unique pathological and clinical features. ARVC is characterized...
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