Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigree

Hereditary non-polyposis colorectal cancer (HNPCC) is the most common genetic susceptibility syndrome for colorectal cancer. HNPCC is most frequently caused by germline mutations in the DNA mismatch repair (MMR) genes MSH2 and MLH1. Recently, mutations in another MMR gene, MSH6 (also known as GTBP), have also been shown to result in HNPCC. Preliminary data indicate that the phenotype related to MSH6 mutations may differ from the classical HNPCC caused by defects in MSH2 and MLH1. Here, we describe an extended Dutch HNPCC family not fulfilling the Amsterdam criteria II and resulting from a MSH6... Mehr ...

Verfasser: Wagner, A. (Anja)
Krimpen, C. (Cees) van
Morreau, H. (Hans)
Hofstra, R.M.W. (Robert)
Tops, C. (Carli)
Cornelisse, C.J. (Cees)
Zwinderman, A.H. (Ailko)
Bik, E.C. (Elsa)
Brocker-Vriends, A.H.
Fodde, R. (Riccardo)
Breuning, M.H. (Martijn)
Meer, C.A. (Conny) van der
Vasen, H.F. (Hans)
Niermeijer, M.F. (Martinus)
Lindhout, D. (Dick)
Hendriks, Y.
Meijers-Heijboer, E.J. (Hanne)
Wijnen, J.T. (Juul)
Leeuw, W.J. de
Dokumenttyp: Artikel
Erscheinungsdatum: 2001
Schlagwörter: Adult / Age of Onset / Aged / 80 and over / Base Pair Mismatch/genetics / Carcinoma / Transitional Cell/epidemiology/genetics/pathology / Colorectal Neoplasms / Hereditary Nonpolyposis/epidemiology/*genetics/pathology / DNA Mutational Analysis / DNA Repair/genetics / DNA-Binding Proteins/*genetics / Diagnosis / Differential / Endometrial Neoplasms/epidemiology/genetics/pathology / Female / Frameshift Mutation/genetics / Genetic Predisposition to Disease/genetics / Genotype / Germ-Line Mutation/*genetics / Humans / Immunohistochemistry / Male / Microsatellite Repeats/genetics / Middle aged / Netherlands / Pedigree / Penetrance / Urologic Neoplasms/epidemiology/genetics/pathology
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-27453292
Datenquelle: BASE; Originalkatalog
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Link(s) : http://repub.eur.nl/pub/9633