Dilated cardiomyopathy (DCM) is a myocardial disorder that is a major cause of heart failure
and death. Recent data indicate that genetic factors are important in the pathogenesis of …

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Dilated cardiomyopathy (DCM) is a myocardial disorder characterised by dilatation and
contractile dysfunction of the left±right ventricles. DCM may be caused by a diverse range of …

Dilated cardiomyopathy (DCM), usually diagnosed as idiopathic dilated cardiomyopathy
(IDC), has been shown to have a familial basis in 20–35% of cases. Genetic studies in …

Dilated cardiomyopathy (DCM) is a myocardial disorder defined by ventricular chamber
enlargement and systolic dysfunction that can result in progressive heart failure …

Genetic disease transmission has been identified in a significant proportion of patients with
dilated cardiomyopathy (DCM). Variable clinical characteristics and patterns of inheritance …

Abstract Purpose of Review Dilated cardiomyopathy (DCM) is characterized by left
ventricular dilation and systolic function and is the most common among all …

Many individuals with DCM do not even consider that they may have an inherited form of the
condition until they begin to analyze their family history. Familial DCM is clinically and …

Idiopathic dilated cardiomyopathy (IDC) is characterized by left ventricular dilatation and
systolic dysfunction after known causes have been excluded. Idiopathic dilated …

Background: It was the aim to investigate the frequency and genetic basis of dilated
cardiomyopathy (DCM) among relatives of index patients with unexplained heart failure at a …