Aims In this study, we aimed to clinically and genetically characterize LVNC patients and
investigate the prevalence of variants in known and novel LVNC disease genes. Introduction …

Background—Left ventricular (LV) noncompaction (LVNC) is a distinct cardiomyopathy
featuring a thickened bilayered LV wall consisting of a thick endocardial layer with …

Left ventricular non‐compaction (LVNC) is a cardiomyopathy that may be of genetic origin;
however, few data are available about the yield of mutation, the spectrum of genes and …

Left ventricular non-compaction (LVNC) is a rare disorder that results in multiple deep
trabeculations within the left ventricular myocardium. It is thought to be due in part, to an …

Introduction Left ventricular non-compaction cardiomyopathy (LVNC) is a rare
cardiomyopathy, originally described as an isolated disease without other structural cardiac …

Background—Left ventricular noncompaction of the myocardium (LVNC) has been
recognized as a cardiomyopathy with a genetic etiology. Mutations in genes encoding …

The first case of noncompaction was described in 1932 after an autopsy performed on a
newborn infant with aortic atresia/coronary–ventricular fistula. Isolated noncompaction …

Aims Left ventricular non-compaction (LVNC) is caused by mutations in multiple genes. It is
still unclear whether LVNC is the primary determinant of cardiomyopathy or rather a …

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

Left ventricular noncompaction (LVNC) is a cardiomyopathy characterized by two layered
structures composed of prominent trabecular meshwork and deep intertrabecular recesses …