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家族性腺瘤性息肉病:疾病多样性和基因异质性的更多证据。

Familial adenomatous polyposis: more evidence for disease diversity and genetic heterogeneity.

作者信息

Scott R J, Meldrum C, Crooks R, Spigelman A D, Kirk J, Tucker K, Koorey D

机构信息

Hunter Area Pathology Service, Locked Bag No 1, Hunter Regional Mail Centre, Newcastle NSW 2310, Australia.

出版信息

Gut. 2001 Apr;48(4):508-14. doi: 10.1136/gut.48.4.508.

Abstract

Familial adenomatous polyposis (FAP) is characterised by the presence of profuse colonic carpeting of adenomas throughout the entire colon and rectum. The genetic basis of FAP has been shown to be primarily associated with germline mutations in the APC gene. Notwithstanding, several reports have been published indicating that there is genetic heterogeneity in FAP and that the most likely explanation is the existence of another gene. In this report we further delineate the genotype/phenotype correlation in families that harbour germline mutations in the APC gene and identify some previously unreported changes in the APC gene which predispose to an attenuated disease phenotype. From 53 index patients diagnosed with either FAP or attenuated FAP, 27 harboured changes in the APC gene. The remaining 26 patients were further subgrouped according to their colonic phenotype. There were nine patients with a mixed hyperplastic/adenomatous colonic phenotype and there were 17 patients with an adenomatous colonic phenotype. Evaluation of the disease characteristics of these patients and their families is presented which may aid in the identification of new genes associated with colonic polyposis.

摘要

家族性腺瘤性息肉病(FAP)的特征是在整个结肠和直肠中存在大量腺瘤性息肉。FAP的遗传基础已被证明主要与APC基因的种系突变有关。尽管如此,已有多篇报道表明FAP存在遗传异质性,最可能的解释是存在另一个基因。在本报告中,我们进一步描述了携带APC基因种系突变的家族中的基因型/表型相关性,并鉴定了一些先前未报道的APC基因变化,这些变化易导致疾病表型减弱。在53例被诊断为FAP或轻度FAP的索引患者中,27例携带APC基因变化。其余26例患者根据其结肠表型进一步分组。有9例患者具有增生性/腺瘤性混合结肠表型,17例患者具有腺瘤性结肠表型。本文介绍了对这些患者及其家族疾病特征的评估,这可能有助于识别与结肠息肉病相关的新基因。

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