Dilated cardiomyopathy (DCM) is a leading cause of heart failure and the most frequent
indication for heart transplantation in young patients. Probably> 25% of DCM cases are of …

Dilated cardiomyopathy (DCM) is a heart-muscle disease characterized by ventricular
dilatation and impaired heart contraction and is heterogeneous both clinically and …

Dilated cardiomyopathy (DCM) is the most common form of primary myocardial disorder,
accounting for 60% of all cardiomyopathies. In 20-30% of cases, familial inheritance can be …

The pathogenesis of dilated cardiomyopathy (DCM) remains controversial. Over the last few
years there has been a gradual accumulation of evidence suggesting that familial forms of …

Genetic bases of dilated cardiomyopathy : Journal of Cardiovascular Medicine Genetic bases
of dilated cardiomyopathy : Journal of Cardiovascular Medicine Log in or Register Subscribe to …

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

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

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 …

Dilated cardiomyopathy (DCM) is a myocardial disease characterized by dilatation and
impaired systolic function of the left or both ventricles. The etiology of DCM is multifactorial …

1757 (Genetic) Genetic Factors in DCM contrast, the genetic factor is composed of multiple
diseaseassociated gene polymorphisms in the multifactorial disease. In general, the …