Contribution of APC and MUTYH mutations to familial adenomatous polyposis susceptibility in Hungary
Familial adenomatous polyposis (FAP) is a colorectal cancer predisposition syndrome with considerable genetic and phenotypic heterogeneity, defined by the development of multiple adenomas throughout the colorectum. FAP is caused either by monoallelic mutations in the adenomatous polyposis coli gene...
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Veröffentlicht in: | Familial cancer 2016-01, Vol.15 (1), p.85-97 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Familial adenomatous polyposis (FAP) is a colorectal cancer predisposition syndrome with considerable genetic and phenotypic heterogeneity, defined by the development of multiple adenomas throughout the colorectum. FAP is caused either by monoallelic mutations in the adenomatous polyposis coli gene APC, or by biallelic germline mutations of MUTYH, this latter usually presenting with milder phenotype. The aim of the present study was to characterize the genotype and phenotype of Hungarian FAP patients. Mutation screening of 87 unrelated probands from FAP families (21 of them presented as the attenuated variant of the disease, showing |
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ISSN: | 1389-9600 1573-7292 |
DOI: | 10.1007/s10689-015-9845-5 |