Hypertrophic obstructive cardiomyopathy and the mitral valve View Full Text


Ontology type: schema:Chapter     


Chapter Info

DATE

2011

AUTHORS

B. Nasseri , C. Stamm , E.M. Delmo Walter , R. Hetzer

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. More... »

PAGES

67-79

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/978-3-7985-1867-4_5

DOI

http://dx.doi.org/10.1007/978-3-7985-1867-4_5

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1005311820


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