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Abstract. Dilated cardiomyopathy (DCM) is best understood as the final common response of myocardium to diverse genetic and environmental insults. A rigorous work-up can exclude alternative causes of left ventricular (LV) dilation and dysfunction, identify etiologies that may respond to specific treatments, and guide family screening.Dilated cardiomyopathy is a type of heart muscle disease that causes the heart chambers (ventricles) to thin and stretch, growing larger. It typically starts in the heart's main pumping chamber (left ventricle). Dilated cardiomyopathy makes it harder for the heart to pump blood to the rest of the body.
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Dilated cardiomyopathy is a progressive disease of heart muscle that is characterized by ventricular chamber enlargement and contractile dysfunction. The right.DCM is defined in the presence of left ventricular (LV) ejection fraction (EF) 2.7 cm/m 2 or >117% predicted value corrected for age and body surface area [ 1, 3, 4 ]. Table 7.1. Echocardiographic features of DCM. The hallmark of the disease is a global LV dilation (Fig. 7.1 ).
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