Abstract
Hypertrophic cardiomyopathy (HCM) is a complex congenital cardiac disease and belongs to the group of cardiomyopathies. The estimated prevalence is 1:500. Although it has unique pathophysiological characteristics, there is a great diversity of functional, clinical, morphological, and molecular findings. Therefore and because of the relatively low prevalence in general practice, therapy management decisions have been derived from nonrandomized and retrospective investigations.
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Nasseri, B., Stamm, C., Delmo Walter, E., Hetzer, R. (2011). Hypertrophic obstructive cardiomyopathy and the mitral valve. In: Hetzer, R., Rankin, J., Yankah, C. (eds) Mitral Valve Repair. Steinkopff. https://doi.org/10.1007/978-3-7985-1867-4_5
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