Inherited cardiomyopathies include hypertrophic cardiomyopathy, dilated cardiomyopathy,
arrhythmogenic right ventricular cardiomyopathy, left ventricular noncompaction, and …

Pediatric cardiomyopathies, which are rare but serious disorders of the muscles of the heart,
affect at least one in every 100,000 children in the USA. Approximately 40% of children with …

1From Mayo Clinic, Rochester, Minnesota; 2Fondazione Salvatore Maugeri University of
Pavia, Pavia, Italy and New York University, New York, New York; 3University Hospital …

Left ventricular noncompaction (LVNC) causes prominent ventricular trabeculations and
reduces cardiac systolic function. The clinical presentation of LVNC ranges from …

Left ventricular non-compaction (LVNC) is a heart-muscle disorder characterized by
prominent myocardial trabeculations and deep intertrabecular recesses in the LV cavity …

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 …

Left ventricular non-compaction (LVNC) describes the phenotypical phenomena
characterized by the presence of excessive trabeculation of the left ventricle which forms a …

Left ventricular noncompaction (LVNC) cardiomyopathy is morphologically characterized by
prominent myocardial trabeculations and deep recesses. The precise stage of development …

Electrophysiological and structural disruptions in cardiac arrhythmias are closely related to
mitochondrial dysfunction. Mitochondria are an organelle generating ATP, thereby satisfying …

Aims Ryanodine receptor gene (RYR2) mutations are well known to cause
catecholaminergic polymorphic ventricular tachycardia (CPVT). Recently, RYR2 exon 3 …