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01-12-2009 | original article

Risk stratification for sudden cardiac death in hypertrophic cardiomyopathy: Dutch cardiologists and the care of mutation carriers

Auteurs: J. T. Vehmeijer, I. Christiaans, I. M. van Langen, E. Birnie, G. J. Bonsel, E. M. A. Smets, A. A. M. Wilde

Gepubliceerd in: Netherlands Heart Journal | Uitgave 12/2009

Extract

With a prevalence of about one in 500, hypertrophic cardiomyopathy (HCM) is one of the most common genetic diseases.1 HCM is inherited as an autosomal dominant trait caused by a large variety of mutations – around 450 different mutations in more than 11 genes have been reported.2 HCM is clinically classified as a (usually asymmetric) thickening of the myocardial wall of the left ventricle, often involving the interventricular septum, which cannot be accounted for by other clinical diseases.3,4 Most patients experience few if any symptoms. If present, symptoms are diverse. Common symptoms are chest pain during exertion and dyspnoea.5 …

vorige artikel Hypertrophic cardiomyopathy family with double-heterozygous mutations; does disease severity suggest doubleheterozygosity?

volgende artikel Reduced regional myocardial perfusion reserve is associated with impaired contractile performance in idiopathic dilated cardiomyopathy

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Titel: Risk stratification for sudden cardiac death in hypertrophic cardiomyopathy: Dutch cardiologists and the care of mutation carriers
Auteurs: J. T. Vehmeijer
I. Christiaans
I. M. van Langen
E. Birnie
G. J. Bonsel
E. M. A. Smets
A. A. M. Wilde
Publicatiedatum: 01-12-2009
Uitgeverij: Bohn Stafleu van Loghum
Gepubliceerd in: Netherlands Heart Journal / Uitgave 12/2009
Print ISSN: 1568-5888
Elektronisch ISSN: 1876-6250
DOI: https://doi.org/10.1007/BF03086305

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