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Number of results
2007 | 48 | 2 | 185-188

Article title

Mutation of the MYH7 gene in a child with hypertrophic cardiomyopathy and Wolff-Parkinson-White syndrome

Title variants

Languages of publication

EN

Abstracts

EN
Familial hypertrophic cardiomyopathy (HCM) displays autosomal dominant inheritance with incomplete penetration of defective genes. Data concerning the familial occurrence of ventricular preexcitation, i.e. Wolff-Parkinson-White (WPW) syndrome, also indicate autosomal dominant inheritance. In the literature, only a gene mutation on chromosome 7q3 has been described in familial HCM coexisting with WPW syndrome to date. The present paper describes the case of a 7-year-old boy with HCM and coexisting WPW syndrome. On his chromosome 14, molecular diagnostics revealed a C 9123 mutation (arginine changed into cysteine in position 453) in exon 14 in a copy of the gene for beta-myosin heavy chain (MYH7). It is the first known case of mutation of the MYH7 gene in a child with both HCM and WPW. Since no linkage between MYH7 mutation and HCM with WPW syndrome has been reported to date, we cannot conclude whether the observed mutation is a common cause for both diseases, or this patient presents an incidental co-occurrence of HCM (caused by MYH7 mutation) and WPW syndrome.

Discipline

Year

Volume

48

Issue

2

Pages

185-188

Physical description

Contributors

author
author
author
author
author
author

References

Document Type

ARTICLE

Publication order reference

W. Bobkowski, Department of Paediatric Cardiology, Poznan University of Medical Sciences, Szpitalna 27/33, 60?572 Poznan, Poland

Identifiers

YADDA identifier

bwmeta1.element.element-from-psjc-c48afff7-9cf7-3f59-ba49-27d346de2be8
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