Long-Term Results in Different Forms of Hypertrophic Cardiomyopathy

Autor: U. Müller, E. R. de Vivie, F. Klostermann, H. Wesselhoeft, J. Vogt, A. J. Beuren, G. Eigster, Rupprath G
Rok vydání: 1986
Předmět:
Zdroj: Pediatric Cardiology ISBN: 9781461386001
DOI: 10.1007/978-1-4613-8598-1_277
Popis: Hypertrophic cardiomyopathy (HCM), which is usually characterized by asymmetric septal hypertrophy and histologically by a severe degree of myocyte hypertrophy and foci of disarray of bundles of myocytes or myocardial fibers, is observed more frequently in adults [1, 2]. Previous detailed reports of HCM in early childhood were limited to single cases or descriptions of only a few patients [3–5].
Databáze: OpenAIRE