Hypertrophic cardiomyopathy (HCM) is the most common heritable cardiomyopathy,
manifesting as left ventricular hypertrophy in the absence of a secondary cause. The genetic …

Hypertrophic cardiomyopathy (HCM) is a global disease with cases reported in all
continents, affecting people of both genders and of various racial and ethnic origins. Widely …

Hypertrophic cardiomyopathy (HCM) is a myocardial dis-order characterized by left
ventricular (LV) hypertrophy without dilatation and without apparent cause (ie, it occurs in …

Hypertrophic cardiomyopathy (HCM) is a heterogeneous group of diseases related to
sarcomere gene mutations exhibiting heterogeneous phenotypes with an autosomal …

Hypertrophic cardiomyopathy (HCM) is a common inherited heart disease with diverse
phenotypic and genetic expression, clinical presentation, and natural history. HCM has been …

Hypertrophic cardiomyopathy (HCM) is a relatively common often inherited global heart
disease, with complex phenotypic and genetic expression and natural history, affecting both …

Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiac disease. The
disease is characterized by marked variability in morphological expression and natural …

Hypertrophic cardiomyopathy (HCM) is the most common inherited heart disease and
defined by unexplained isolated progressive myocardial hypertrophy, systolic and diastolic …

Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiovascular disorder,
affecting 1 in 500 individuals worldwide. Existing epidemiological studies might have …

Hypertrophic cardiomyopathy (HCM) is the most common monogenic heart disease with a
frequency as high as 1 in 200. In many cases, HCM is caused by mutations in genes …