Kardiomiopatie definiuje się jako strukturalne oraz funkcjonalne nieprawidłowości mięśnia
komór, które nie wynikają z niedokrwienia na skutek choroby wieńcowej czy …

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

Hypertrophic cardiomyopathy, one of the most common genetic cardiovascular conditions,
will be encountered by nearly every health-care provider regardless of specialty. In 2020 …

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

Heart: first published as 10.1136/heart. 86.6. 709 on 1 December 2001. Downloaded from
heart disease at a relatively young age, HCM is a distinct possibility. That possibility is …

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

Hypertrophic cardiomyopathy is a complex and relatively common genetic cardiac disorder
(about 1: 500 in the general adult population) 1that has been the subject of intense scrutiny …

Hypertrophic cardiomyopathy (HCM) is a clinically and genetically heterogeneous disorder
but data on survival rates are still conflicting and have not so far been quantitatively …

Hypertrophic cardiomyopathy (HCM) is an inherited cardiac muscle disorder disease that
affects sarcomeric proteins, resulting in small vessel disease, myocyte and myofibrillar …

Methods In this article, we summarize the current state of the diagnosis and treatment of
HCM on the basis of a selective review of recent publications with relevance to clinical …