Abstract
In 1907 Schmincke [93] was the first to describe diffuse “hyperplasia” of the heart muscle, involving predominantly the wall of the left ventricular outflow tract, in two female patients. In 1958 Teare [104] presented pathologic findings of asymmetrical hypertrophy of the heart in young adults, eight of whom died from sudden death, seven of them during physical activity. In 1964 Braunwald et al. [9] described the findings in 64 patients with hypertrophic cardiomyopathy (HCM), emphasizing angiographically determined normal or even supernormal left ventricular function and hemodynamically documented large variations of outflow tract gradient. Today, there seems to be no doubt that impaired diastolic function of the left ventricle is the predominant hemodynamic characteristic in HCM [106, 107].
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Hopf, R., Kaltenbach, M. (1990). Medical Treatment of Hypertrophic Cardiomyopathy. In: Baroldi, G., Camerini, F., Goodwin, J.F. (eds) Advances in Cardiomyopathies. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-83760-9_12
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