[Multiple abnormalities in a child with male karyotype due to familial partial Xp duplication].

Kinderarztliche Praxis Pub Date : 1993-10-01
H Reichenbach, H Holland, B Thamm, T Theile
{"title":"[Multiple abnormalities in a child with male karyotype due to familial partial Xp duplication].","authors":"H Reichenbach,&nbsp;H Holland,&nbsp;B Thamm,&nbsp;T Theile","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>A child with multiple abnormalities and intersexual external genitals is presented. The child has a male karyotype with a partial duplication Xp. Using additionally methods of molecular genetics the SRY-region was detected. We reviewed the only few persons described in the literature with male karyotype and partial duplications Xp. There are similarities in phenotype including sex inversion or intersexual genitals if the duplication is localised in the region Xp 21-->Xp 22. Whether these affected patients represent a new syndrome is a moot point. We also found the aberrant X-chromosome in the mother of the child. In the present pregnancy of the mother there is, therefore, a risk of recurrence.</p>","PeriodicalId":76073,"journal":{"name":"Kinderarztliche Praxis","volume":"61 7-8","pages":"291-5"},"PeriodicalIF":0.0000,"publicationDate":"1993-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Kinderarztliche Praxis","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

A child with multiple abnormalities and intersexual external genitals is presented. The child has a male karyotype with a partial duplication Xp. Using additionally methods of molecular genetics the SRY-region was detected. We reviewed the only few persons described in the literature with male karyotype and partial duplications Xp. There are similarities in phenotype including sex inversion or intersexual genitals if the duplication is localised in the region Xp 21-->Xp 22. Whether these affected patients represent a new syndrome is a moot point. We also found the aberrant X-chromosome in the mother of the child. In the present pregnancy of the mother there is, therefore, a risk of recurrence.

分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
[家族性部分Xp重复引起的男性核型儿童的多重异常]。
一个患有多种异常和雌雄间性外生殖器的儿童。孩子的核型为男性,部分重复Xp。另外利用分子遗传学方法对sry区进行检测。我们回顾了文献中仅有的几个男性核型和部分重复Xp的人。如果复制定位于Xp 21- >Xp 22区域,则在表型上存在相似之处,包括性反转或两性间生殖器。这些受影响的患者是否代表一种新的综合征尚无定论。我们还在孩子的母亲身上发现了异常的x染色体。因此,在母亲目前的怀孕中,有复发的危险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
[Bronchopulmonary dysplasia]. [The pathogen spectrum of blood cultures of premature and newborn infants in a neonatal intensive care unit]. [Use of the Glasgow Coma Scale in pediatric craniocerebral trauma]. [15N liver function test in underweight infants, hypotrophic at birth]. [Ondine syndrome: presentation of pediatric aspects based on a case report].
wanfang
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1