Aim. To study and compare genotypic and phenotypic signs in patients with non-compaction
cardiomyopathy (NCM) and dilated cardiomyopathy (DCM), to conduct a comparative …

Improvement of high-tech methods of cardiac imaging and new generation sequencing with
their introduction into widespread practice has significantly expanded the potential of …

Background: There is overlap in genetic causes and cardiac features in noncompaction
cardiomyopathy (NCCM), hypertrophic cardiomyopathy (HCM), and dilated cardiomyopathy …

diology and the American Heart Association indicate the existence of several phenotypes of
myocardial non-compaction (MnC) with specific structural and functional abnormalities. The …

Objective: Isolated noncompaction cardiomyopathy (NCCM) is considered a primary genetic
cardiomyopathy. Smaller studies suggest that the prognosis of pts with NCCM is determined …

Background: The clinical outcomes of noncompaction cardiomyopathy (NCCM) range from
asymptomatic to heart failure, arrhythmias, and sudden cardiac death. Genetics play an …

Aims Left ventricular non‐compaction cardiomyopathy (LVNC) is a poorly understood entity
resulting in heart failure. Whether it is a distinct form of cardiomyopathy or an anatomical …

Background Noncompaction cardiomyopathy (NCCM) is characterized by a thickened
myocardial wall with excessive trabeculations of the left ventricle, and∼ 30% is explained by …

Objective: Isolated noncompaction cardiomyopathy (NCCM) is considered a primary genetic
cardiomyopathy associated with heart failure (HF), arrhythmias, and thrombembolic events …

Background Isolated noncompaction cardiomyopathy (NCCM) is considered a primary
genetic cardiomyopathy. The clinical outcome of the affected patients (pts) varies …