Heart failure (HF) is a complex clinical syndrome resulting from diverse primary and
secondary causes and shared pathways of disease progression, correlating with substantial …

Ebstein's anomaly is uncommon. Genetic bases of this congenital heart defect may be
related to the mutations in myosin heavy chain 7 and NKX2. 5, among others. Asymptomatic …

ObjectivesThe aim of this study was to describe the epidemiology of Ebstein's anomaly in
Europe and its association with maternal health and medication exposure during pregnancy …

Left ventricular noncompaction cardiomyopathy (LVNC) is a myocardial disorder
characterized by prominent and excessive trabeculations with deep recesses in the …

Background The non-POU domain containing octamer-binding gene (NONO) is located on
chromosome Xq13. 1 and encodes a member of a small family of RNA-binding and DNA …

Background Mutations in the myosin heavy chain 7 (MYH7) gene commonly cause
cardiomyopathy but are less frequently associated with congenital heart defects. Methods In …

2 Hershberger et al Left Ventricular Noncompaction 1480 individuals from the UK-Canadian
TASCFORCE study (Tayside Screening for Cardiac Events), also identified LVNC as a …

Background—Familial Ebstein anomaly is a rare form of congenital heart disease. We report
7 individuals among 2 generations of 1 family with Ebstein anomaly. This family was first …

Congenital heart disease is a major health issue, accounting for a third of all congenital
defects. Improved early surgical management has led to a growing population of adults with …

Background Ebstein anomaly (EA) is a rare congenital defect characterized by apical
displacement of the septal tricuspid leaflets and atrialization of the right ventricle. The …