Suppr超能文献

[一名患有18q21部分单体综合征的女孩:细胞遗传学和分子遗传学研究]

[A girl with partial monosomy 18q21: cytogenetic and molecular genetics studies].

作者信息

Lu Hong-Yong, Cui Ying-Xia, Shi Yi-Chao, Xia Xin-Yi, Yang Bin, Yao Bing, Huang Yu-Feng

机构信息

Medical Technology School of Jiangsu University, Zhenjiang 212013, China.

出版信息

Yi Chuan. 2008 Aug;30(8):991-5. doi: 10.3724/sp.j.1005.2008.00991.

Abstract

This study is about a girl with chromosome deletion of 18q and with mental retardation and mild delay of physical development. Based on karyotyping of high resolution, fluorescence in situ hybridization (FISH) and microsatellite analysis mapping to 18q, we found that the patient's karyotype was interpreted as 46,XX,del(18).(pter-->q21:), ish del(18)(D18Z1+,qter-). Detection of D18S979 showed that the region from 18q21.1 to 18qter was deleted, which was originated from her father. There were MBP gene and GALNR gene in the deleted interval in which both of them were lost. In conclusion, deletion of 18q21-->qter including the MBP gene and GALNR gene should be responsible for her mental retardation and mild delay of development.

摘要

本研究涉及一名患有18q染色体缺失、智力发育迟缓且身体发育轻度延迟的女孩。基于高分辨率核型分析、荧光原位杂交(FISH)以及定位到18q的微卫星分析,我们发现该患者的核型被解释为46,XX,del(18).(pter→q21:), ish del(18)(D18Z1+,qter-)。对D18S979的检测表明,18q21.1至18qter区域缺失,该缺失源自她的父亲。缺失区间内存在MBP基因和GALNR基因,二者均缺失。总之,18q21→qter的缺失,包括MBP基因和GALNR基因,应是导致她智力发育迟缓和发育轻度延迟的原因。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验