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肛门直肠畸形病因中的染色体异常:综述。

Chromosomal anomalies in the etiology of anorectal malformations: a review.

机构信息

Department of Human Genetics, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.

出版信息

Am J Med Genet A. 2011 Nov;155A(11):2692-704. doi: 10.1002/ajmg.a.34253. Epub 2011 Oct 11.

Abstract

Anorectal malformation (ARM) is a severe congenital anomaly that can occur either isolated or in association with other congenital abnormalities. It has a heterogeneous etiology with contribution of both genetic and environmental factors, although the etiological factors remain largely unknown. Several chromosomal abnormalities have been described in patients with an ARM. These chromosomal abnormalities could point to specific genes involved in the development of the anorectal canal and associated structures. This paper reviews the chromosomal abnormalities described in ARM and may act as a starting point to identify chromosomal regions containing putative anorectal development genes.

摘要

肛门直肠畸形(ARM)是一种严重的先天性异常,可单独发生或与其他先天性异常相关。它的病因具有异质性,遗传和环境因素都有贡献,尽管病因仍很大程度上未知。在患有 ARM 的患者中已经描述了几种染色体异常。这些染色体异常可能指向参与肛门直肠管和相关结构发育的特定基因。本文综述了在 ARM 中描述的染色体异常,可能成为鉴定包含推定肛门直肠发育基因的染色体区域的起点。

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