Determinants of LV Dilatation in Patients With Hypertrophic Cardiomyopathy and Preserved Systolic Function: A CMR Study

Hypertrophic cardiomyopathy (HCM) is a genetic disorder characterized by left ventricular (LV) hypertrophy in the absence of another disease state. HCM is commonly associated with either normal or small LV volumes ([1][1]) or with LV dilatation described as end-stage disease associated with