Abstract
Hypertrophic cardiomyopathy (HCM) is a complex disease of multiple genetic origins. It is usually a familial cardiac disorder, recognised to be of heterogeneous expression with diverse clinical manifestations and outcome. This structural and functional abnormality of the myocardium is the phenotype of many genetic disorders of encoding proteins of the sarcomere. The diagnostic disorder is a thickened and non-dilated left ventricle in the absence of an associated condition that could explain the hypertrophy.
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Kappenberger, L.J., Aebischer, N., Jeanrenaud, X. (2000). Pacemaker Treatment for Hypertrophic Obstructive Cardiomyopathy: Are Long-Term Results as Good as Short-Term Ones?. In: Raviele, A. (eds) Cardiac Arrhythmias 1999. Springer, Milano. https://doi.org/10.1007/978-88-470-2139-6_69
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DOI: https://doi.org/10.1007/978-88-470-2139-6_69
Publisher Name: Springer, Milano
Print ISBN: 978-88-470-2178-5
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