Cardiomyopathies are defined as disorders of the myocardium which are always associated
with cardiac dysfunction and are aggravated by arrhythmias, heart failure and sudden death …

Cardiac manifestations in hereditary muscle diseases include cardiomyopathies, defects of
cardiac conductions with or without primary myocardial muscle involvement, and …

Cardiomyopathy classification has been subject to revisions for> 60 years. The new MOGE
(S) classification system, which incorporates information on structural and functional …

Most cardiomyopathies are familial diseases. Cascade family screening identifies
asymptomatic patients and family members with early traits of disease. The inheritance is …

In 1956, Blankerhorn and Gall (1) proposed the term myocarditis for inflammatory heart
muscle disease, and myocardiosis for other heart muscle diseases. A year thereafter …

Cardiomyopathies can be defined as disorders of the myocardium which are associated with
cardiac dysfunction and are aggravated by arrhythmias, heart failure and sudden death …

Cardiomyopathies are an important and diverse group of heart muscle diseases in which the
heart muscle itself is structural or functional abnormal. This often results in severe heart …

The term “cardiomyopathies” was used for the first time 55 years ago, in 1957. Since then
awareness and knowledge of this important and complex group of heart muscle diseases …

Cardiomyopathies are defined as diseases of the myocardium with associated structural and
functional abnormalities. Knowledge of these pathologies for a long period was not clear in …

Cardiomyopathy is a disease of the heart muscle resulting from genetic defects, cardiac
myocyte injury, or infiltration of the myocardium. Cardiomyopathies are traditionally defined …