Abstract
Hypertrophic cardiomyopathy (HCM) is a genetic disorder characterized by ventricular hypertrophy in the absence of an identifiable cause for the hypertrophy (1–4). The hypertrophy is usually asymmetric and involves the interventricular septum in 90% of patients. Most commonly, the outflow septum (i.e., subaortic area) is the major focus of hypertrophy, but the midventricular or apical septum may occur in isolation or concomitantly. Rarely (5%) the right ventricle is involved. The extent of the hypertrophy varies tremendously and accounts for different manifestations of the disease (1–5). The hypertrophy is associated with myocardial fiber disarray on microscopy.
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Williams, W.G., Wigle, E.D., Rakowski, H., Ralph-Edwards, A.C., Schwartz, L. (2005). Surgical Management of Hypertrophic Cardiomyopathy. In: Fang, J.C., Couper, G.S. (eds) Surgical Management of Congestive Heart Failure. Contemporary Cardiology. Humana Press. https://doi.org/10.1385/1-59259-842-0:203
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DOI: https://doi.org/10.1385/1-59259-842-0:203
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