—Dr. Wang spoke to MedPage Today to discuss the diagnosis of apical HCM, and distinct features of this disease subtype. Apical hypertrophic cardiomyopathy (HCM) is a morphological subtype of HCM that ...
Hypertrophic cardiomyopathy (HCM) is a heterogeneous monogenic heart disease of unknown origin characterized by asymmetric hypertrophy of the ventricular wall 1. Mutations in genes encoding the ...
Future Cardiol. 2013;9(5):697-709. It is extremely important to detect the presence and severity of LVOT obstruction from physical examination, as well as 2D and Doppler echocardiography. The LVOT ...
Hypertrophic cardiomyopathy (HCM), the most common inherited cardiomyopathy, is characterized by phenotypic and genetic heterogeneity. The present study describes the genotype data of a Swedish cohort ...
HCM is a primary disease of cardiac muscle characterized by a thickening of the LV wall and often predominantly affecting the interventricular septum. HCM is a genetic disease with an autosomal ...
Aim Differentiating physiological cardiac hypertrophy from pathology is challenging when the athlete presents with extreme anthropometry. While upper normal limits exist for maximal left ventricular ...
Credit: Getty Images HCM is a genetic disease, usually caused by mutations in sarcomere proteins such as myosin, actin, tropomyosin, and myosin-binding protein C. Hypertrophic cardiomyopathy (HCM) ...
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