Zusammenfassung
In der älteren Literatur wurden Kardiomyopathien als „Erkrankungen des Herzmuskels unklarer Ätiologie“ definiert und von spezifischen Herzmuskelerkrankungen bekannter Ätiologie abgegrenzt. Entsprechend ihrer charakteristischen anatomischen Veränderungen, unterschiedlicher klinischer Verläufe und variierender zur Erkrankung führender und diese unterhaltender pathophysiologischer Mechanismen wurden sie in dilatative, hypertrophe, restriktive und nicht klassifizierbare Kardiomyopathien eingeteilt.
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Schultheiss, HP. (1999). Kardiomyopathien. In: Paumgartner, G., et al. Therapie innerer Krankheiten. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-10477-4_2
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