Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiomyopathy. It
follows an autosomal dominant inheritance pattern in most cases, with incomplete …

Purpose: To evaluate the left atrial (LA) function in participants with apical hypertrophic
cardiomyopathy (AHCM) by cardiovascular magnetic resonance feature tracking (CMR-FT) …

Background Hypertrophic cardiomyopathy (HCM), one of the most common genetic
cardiovascular diseases, but cannot be explained by single genetic factors. Circulating …

Background. Hypertrophic cardiomyopathy (HCM) in pediatric solid organ transplant
recipients has been reported in association with use of calcineurin inhibitors. However, data …

Obstructive hypertrophic cardiomyopathy (oHCM) and mitral valve (MV) prolapse (MVP) are
the 2 conditions which could cause symptomatic heart failure and sudden cardiac death …

Background Familial hypertrophic cardiomyopathy (HCM) is the most common genetic
cardiovascular disease. Related mutations contributing to hypercontractility and poor …

Reports on the treatment of nonobstructive hypertrophic cardiomyopathy (HCM) and severe
mitral valve regurgitation (MR) with transcatheter edge‐to‐edge repair (TEER) are rare …

Hypertrophic cardiomyopathy (HCM) is the most prevailing heritable cardiomyopathy. HCM
is diagnosed by the existence of left ventricular hypertrophy despite the lack of abnormal …

Hypertrophic cardiomyopathy (HCM) is an inherited cardiovascular disease characterized
by left ventricular hypertrophy and a high risk of sudden death. In this study, a skin biopsy …

Hypertrophic cardiomyopathy (HCM) is among the most common forms of cardiomyopathies,
with a prevalence of 1: 200 to 1: 500 people. HCM is caused by variants in genes encoding …