Noncompaction cardiomyopathy (NCCM) has gained increasing attention over the past
twenty years, but in daily clinical practice NCCM is still rarely considered. So far, there are …

Inherited cardiomyopathies are a major cause of mortality and morbidity worldwide and can
be caused by mutations in a wide range of proteins located in different cellular …

Background: Left ventricular noncompaction (LVNC) is a hereditary cardiomyopathy that is
associated with high morbidity and mortality rates. Recently, LVNC was classified into …

The remodeling of the compact wall by incorporation of trabecular myocardium, referred to
as compaction, receives much attention because it is thought that its failure causes left …

Abstract Sudden Infant Death syndrome (SIDS) is a diagnosis of exclusion. Decades of
research have made steady gains in understanding plausible mechanisms of terminal …

Practical relevance: Although feline hypertrophic cardiomyopathy (HCM) occurs more
commonly, dilated cardiomyopathy (DCM), restrictive cardiomyopathy (RCM) …

Background: Left ventricular noncompaction cardiomyopathy (LVNC) is a rare cardiac
disorder characterised by the presence of a two-layer myocardium with prominent …

Background Left ventricular noncompaction cardiomyopathy (LVNC) is a hereditary heart
disease characterized by an excessive trabecular meshwork of deep intertrabecular …

Background Left ventricular noncompaction (LVNC) cardiomyopathy is a disorder that can
be complicated by heart failure, arrhythmias, thromboembolism, and sudden cardiac death …

Background Left ventricular non-compaction cardiomyopathy (LVNC) is a rare congenital
heart defect. Gene defections have been found in patients with LVNC and their family …