Background: Hypertrophic Cardiomyopathy (HCM) is one of the leading causes sudden cardiac death in adults.HCM inherited an autosomal dominant manner; however, genetic etiology disease not fully explained and studies on hereditary characteristics family trees are still underway. Methods: Ten HCM patients 31 their relatives were recruited. Targeted sequencing for 4 related-genes, including MYH7 ,...

Abstract Introduction In the last few years, genetic investigation has become an active part of diagnostic and therapeutic pathway cardiological patients with cardiomyopathies. Genetic assumes a key role in clinical–decision–making process proband acquiring potential changing clinical action. Patients referred for screening are affected by hypertrophic, arrhythmogenic dilated cardiomyopathy. fo...