Dilated cardiomyopathy (DCM) is the most common form of cardiomyopathy and one of the
most common causes of heart failure. It is characterized by left or biventricular dilation and a …

Since initial pathologic descriptions in the 1920s, LVNC has been identified in association
with a variety of congenital heart malformations or metabolic syndromes. 1–4 More recently …

Atrial fibrillation (AF) often complicates the course of inherited cardiomyopathies and, in
some cases, may be the presenting feature. Each inherited cardiomyopathy has its own …

Left ventricular noncompaction (LVNC) is an increasingly recognised cardiomyopathy
characterised by excessive trabeculation and deep intertrabecular recesses in direct …

In the very young child (less than eight years of age), transient loss of consciousness
represents a diagnostic and management dilemma for clinicians. While most commonly …

Left ventricular noncompaction (LVNC) is a type of cardiomyopathy characterized
anatomically by prominent ventricular trabeculation and deep intertrabecular recesses. The …

Некомпактный («губчатый») миокард (НКМ)—генетически гетерогенная первичная
кардиомиопатия, которая встречается как у детей, так и у взрослых, может быть …

Background Non‐compaction cardiomyopathy (NCCM) is a form of structural heart disease
prone to ventricular arrhythmias (VAs) and sudden cardiac death. Non‐compacted …

A 36-year-old man had a markedly dilated left ventricle, an ejection fraction of 20%, and a
diagnosis of noncompaction of the ventricular myocardium [1–22]. In 2004 he had received …

Left ventricular noncompaction cardiomyopathy (LVNC) is a structural heart defect that has
been associated with generation of arrhythmias in the population and is a cause of sudden …