Arrhythmogenic cardiomyopathy (ACM) is a genetically determined heart muscle disease
characterized by fibro-fatty myocardial replacement, clinically associated with malignant …

Arrhythmogenic cardiomyopathy (ACM) is an inherited heart muscle disease characterized
by loss of ventricular myocardium and fibrofatty replacement, which predisposes to scar …

Aims Low QRS voltages (peak to peak< 0.5 mV) in limb leads (LQRSV) on the athlete's
electrocardiogram (ECG) may reflect an underlying cardiomyopathy, mostly arrhythmogenic …

Nonischemic cardiomyopathies include a wide range of dilated, hypertrophic and
arrhythmogenic heart muscle disorders, not explained by coronary artery disease …

Premature ventricular beats (PVBs) in athletes are not rare. The risk of PVBs depends on the
presence of an underlying pathological myocardial substrate predisposing the subject to …

Arrhythmogenic cardiomyopathy (ACM) is a genetic heart muscle disease, structurally
characterized by progressive fibro‐fatty replacement of the normal myocardium and …

Noncoding RNAs (ncRNAs) play an important regulatory role in the activity of genes
essential for the development and functioning of cardiovascular system. Intragenic ncRNAs …

Cardiomyopathies are an actively investigated clinically and genetically heterogeneous
group of myocardial pathologies. At present, it is acknowledged that along with genetic …

Arrhythmogenic Cardiomyopathy (AC), an inherited cardiac disorder characterized by
myocardial fibrofatty replacement, carries a significant risk of sudden cardiac death (SCD) …

The review analyses the scope of the genes of Mendelian cardiomyopathies (CM),
specifically hypertrophic, dilated, arrhythmogenic, and restrictive cardiomyopathy. According …