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雄激素不敏感伴智力障碍:一种相邻基因综合征?

Androgen insensitivity with mental retardation: a contiguous gene syndrome?

作者信息

Davies H R, Hughes I A, Savage M O, Quigley C A, Trifiro M, Pinsky L, Brown T R, Patterson M N

机构信息

Department of Paediatrics, University of Cambridge, UK.

出版信息

J Med Genet. 1997 Feb;34(2):158-60. doi: 10.1136/jmg.34.2.158.

Abstract

We present data to suggest the existence of a mental retardation (MR) locus at Xq11.2-q12 between DXS1 and DXS905, identified in two subjects with complete androgen insensitivity syndrome (CAIS) and MR. Androgen insensitivity syndrome is a disorder of male sexual differentiation caused by a defect in the androgen receptor (AR) gene (Xq11-q12). Two subjects with CAIS resulting from a complete deletion of the AR gene have previously been reported, one of whom also has MR. We have identified another mentally retarded person with a complete deletion of the AR gene. The deletion in the two patients with CAIS and MR extends past the AR gene and includes several marker loci both proximal and distal to the AR gene, the limits of the deletions being DXS1 and DXS905. The deletions in the CAIS patients who do not have MR do not include any of the markers outside the AR gene itself. These data suggest that located close to the AR gene is a gene which is implicated in non-specific MR.

摘要

我们提供的数据表明,在DXS1和DXS905之间的Xq11.2-q12存在一个智力迟钝(MR)基因座,这是在两名患有完全雄激素不敏感综合征(CAIS)和智力迟钝的患者中发现的。雄激素不敏感综合征是一种由雄激素受体(AR)基因(Xq11-q12)缺陷引起的男性性分化障碍。先前已报道过两名因AR基因完全缺失而导致CAIS的患者,其中一名也患有智力迟钝。我们又发现了一名AR基因完全缺失的智力迟钝者。这两名患有CAIS和智力迟钝的患者的缺失延伸至AR基因之外,包括AR基因近端和远端的几个标记基因座,缺失的界限为DXS1和DXS905。没有智力迟钝的CAIS患者的缺失不包括AR基因本身之外的任何标记。这些数据表明,靠近AR基因的位置存在一个与非特异性智力迟钝有关的基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a58/1050872/e39b9ec1cf72/jmedgene00244-0071-a.jpg

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