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18q部分单体患儿的细胞和分子遗传学研究
引用本文:卢洪涌,崔英霞,史轶超,夏欣一,杨滨,姚兵,黄宇烽. 18q部分单体患儿的细胞和分子遗传学研究[J]. 遗传, 2008, 30(8): 991-995. DOI: 10.3724/SP.J.1005.2008.00991
作者姓名:卢洪涌  崔英霞  史轶超  夏欣一  杨滨  姚兵  黄宇烽
作者单位:1. 江苏大学医学技术学院, 镇江 212013;2. 南京军区南京总医院检验医学研究所中心实验科, 南京 210002 ;
基金项目:江苏省卫生厅"135工程"重点学科基金
摘    要:临床发现1例智力低下伴轻度发育迟缓的女性患儿,对患儿进行G显带高分辨染色体核型分析, 发现18q21→qter缺失, 经多色荧光原位杂交和双色荧光原位杂交证实, 确定其核型为46,XX,del(18)(pter→q21:),ish del(18)(D18Z1+, qter-)。用DNA多态性方法分析, 该患儿从18q22.1至18qter区域内至少有8.7 Mbp丢失, 有MBP基因和GALNR基因缺失。缺失的18号染色体源自父亲。患者的智力低下和生长发育迟缓是18q21→qter缺失的结果, 或许与MBP基因和GALNR基因的缺失有关。

关 键 词:染色体  末端缺失  发育迟缓  荧光原位杂交  
收稿时间:2007-12-18
修稿时间:2008-01-23

A girl with partial monosomy 18q21: cytogenetic and molecular ge-netics studies
LU Hong-Yong,CUI Ying-Xia,SHI Yi-Chao,XIA Xin-Yi,YANG Bin,YAO Bing,HUANG Yu-Feng. A girl with partial monosomy 18q21: cytogenetic and molecular ge-netics studies[J]. Hereditas, 2008, 30(8): 991-995. DOI: 10.3724/SP.J.1005.2008.00991
Authors:LU Hong-Yong  CUI Ying-Xia  SHI Yi-Chao  XIA Xin-Yi  YANG Bin  YAO Bing  HUANG Yu-Feng
Affiliation:1. Medical Technology School of Jiangsu University, Zhenjiang 212013, China;2. Institute of Clinical Laboratory Medicine, Department of Clinical Experiment Medicine, Nanjing General Hospital of Nanjing Command, PLA, Nanjing 210002, China ;
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, florescence 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 re-tardation and mild delay of development.
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