Hypertrophic cardiomyopathy: diagnosis, risk stratification and treatment

Abstract excerpt

Hypertrophic cardiomyopathy is a common inherited cardiomyopathy, occurring in about 1 in 500 individuals.[1][1] The first gene mutation for this condition was identified in a large French Canadian family cohort in 1989.[2][2] Clinical presentation typically includes left ventricular hypertrophy in

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