Article
Hypertrophic Cardiomyopathy from A to Z: Genetics, Pathophysiology, Imaging, and Management
1 Mar 2016
Abstract excerpt
Hypertrophic cardiomyopathy (HCM) is a heterogeneous group of diseases related to sarcomere gene mutations exhibiting heterogeneous phenotypes with an autosomal dominant mendelian pattern of inheritance. The disorder is characterized by diverse phenotypic expressions and variable natural progression, which may range from dyspnea and/or syncope to sudden cardiac death. It is found across all racial groups and is...
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