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Thromb Haemost. 2001 Jun;85(6):986-8.

High prevalence of the I278T mutation of the human cystathionine beta-synthase detected by a novel screening application.

Author information

1
Klinik und Poliklinik für Kinderheilkunde, Westfällische Wilhelms-Universität Münster, Germany.

Abstract

Classical homocystinuria due to cystathionine beta-synthase deficiency is one of the disorders revealing a high risk of thromboembolic events and vascular disease. This autosomal-recessively inherited metabolic disorder is considered to be rare with an estimated prevalence of 1:130,000 in the German population. In this study, we developed a novel multiplex PCR generating allele specific fragment lengths to analyse individual genotypes of the two most frequent cystathionine beta-synthase alterations, the I278T mutation, which is worldwide found on up to the half of homocystinuric alleles, and the adjacent polymorphism 844ins68. Screening of 200 unrelated German control subjects revealed a frequency of heterozygosity of 1.5% for 1278T corresponding to a calculated frequency of homozygosity of 1:17.800. Our data indicate that homocystinuria due to cystathionine beta-synthase deficiency is a frequently unrecognized disorder resulting in a high risk of thromboembolic events.

PMID:
11434706
[Indexed for MEDLINE]

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