Hypertrophic cardiomyopathy

The purpose of this study is to study the effect of hypertrophic cardiomyopathy (HCM) on the human body. Hypertrophic cardiomyopathy (HCM) is the most common genetic heart disease. It is a common etiological factor in sudden cardiac death in young people and a common cause of morbidity and mortality in all age groups. HCM is an autosomal dominant disease characterized by hypertrophy (thickening) of the wall of the left and/or occasionally the right ventricle. HCM is characterized by a complex pathophysiology, which is manifested by a heterogeneous clinical picture and is of particular interest for its detailed study.