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按癌症部位进行的基因检测:结肠(息肉综合征)。

Genetic testing by cancer site: colon (polyposis syndromes).

机构信息

Huntsman Cancer Institute, Salt Lake City, UT 84112, USA.

出版信息

Cancer J. 2012 Jul-Aug;18(4):328-33. doi: 10.1097/PPO.0b013e3182609300.

Abstract

Hereditary colonic polyposis conditions are all characterized by high rates of cancer, but they have diverse phenotypes, genetic heterogeneity, and assorted inheritance patterns. The most well known of these conditions include familial adenomatous polyposis, attenuated familial adenomatous polyposis, MUTYH (MutY human homolog)-associated polyposis, Peutz-Jeghers syndrome, juvenile polyposis syndrome, and Cowden syndrome. Early recognition of these conditions is not only vital for management in affected individuals, but also for prevention and early detection in at-risk relatives. Reviewed here are the genetic testing strategies for colonic polyposis, as well as an overview of characteristic features and management considerations for these syndromes.

摘要

遗传性结直肠息肉病的特点是癌症发生率高,但具有不同的表型、遗传异质性和各种遗传模式。其中最著名的疾病包括家族性腺瘤性息肉病、家族性腺瘤性息肉病低危型、MUTYH(MutY 人类同源物)相关息肉病、Peutz-Jeghers 综合征、幼年性息肉病综合征和 Cowden 综合征。早期识别这些疾病不仅对受累个体的管理至关重要,而且对高危亲属的预防和早期发现也至关重要。本文回顾了结直肠息肉病的基因检测策略,并概述了这些综合征的特征和管理注意事项。

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