Cardiology & Vascular Research
- ISSN: 2577-655X
Dev Desai and Siddharth Agarwal
Characterised by ventricular chamber enlargement and systolic dysfunction, dilated cardiomyopathy (DCM) is a heterogeneous disorder with a strong predisposition for genetic mutations. In this review, we provide a synopsis on the etiological perspective of DCM paired with the part genetic testing plays in diagnostics, prophecy, and treatment before emphasising certain genetic tests available and their medically measurable implications.