• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

印度青春期女孩的X染色体异常

X chromosomal abnormalities in Indian adolescent girls.

作者信息

Ganguly Bani Bandana, Sahni Sumedha

机构信息

Cytogenetics Division, Clinical Reference Laboratories, SRL Ranbaxy Ltd., Mumbai, India.

出版信息

Teratog Carcinog Mutagen. 2003;Suppl 1:245-53. doi: 10.1002/tcm.10052.

DOI:10.1002/tcm.10052
PMID:12616615
Abstract

In girls of adolescent age, primary amenorrhea is a major problem and it is often suspected as Turner syndrome (TS), with complete or partial absence of one of the two X chromosomes. The girls who are unable to menstruate are primarily investigated by the gynecologists with the help of a physical examination, sonogram of the pelvis, endocrinologic tests, and ultimately cytogenetic analysis. Chromosomal analyses have been carried out in 280 such cases that were referred from different parts of the country. The standard protocol for peripheral blood lymphocyte culture was followed for metaphase chromosome preparation and conventional analysis of G-banded chromosomes. A total of 29% cases were found to have some chromosomal abnormality, including TS and testicular feminization syndrome involving sex chromosomes. Amongst those with sex chromosomal anomaly, 34% had evidence of a 46,XY karyotype in phenotypic females and 51% had pure line 45,X or mosaic with normal XX or other aberrations in X. The classification of the TS group further showed the spectrum of variant TS in Indian adolescent girls who suffered from absence or delayed menarche to correspond well with the Belgian, Danish, or Russian population. However, it has been reported that only 1% of the pure line 45,X conception is viable, indicating the necessity of mosaicism with X or Y chromosome. It has been understood that conventional banding analysis is absolutely necessary for segregating the variant nature of TS. In addition, molecular genetic or molecular cytogenetic investigations can determine the nature of mosaicism. The present study further indicated the involvement of autosomes in causing improper sexual development in girls of adolescent age.

摘要

在青春期女孩中,原发性闭经是一个主要问题,常被怀疑为特纳综合征(TS),即两条X染色体中的一条完全或部分缺失。无法月经来潮的女孩主要由妇科医生借助体格检查、盆腔超声检查、内分泌检查,最终进行细胞遗传学分析来进行检查。对来自该国不同地区的280例此类病例进行了染色体分析。遵循外周血淋巴细胞培养的标准方案制备中期染色体并进行G带染色体的常规分析。共发现29%的病例存在一些染色体异常,包括涉及性染色体的TS和睾丸女性化综合征。在那些性染色体异常的病例中,34%在表型女性中存在46,XY核型的证据,51%有纯合子45,X或与正常XX或其他X染色体畸变的嵌合体。TS组的分类进一步表明,在印度青春期女孩中,患有月经初潮缺失或延迟的变异TS谱与比利时、丹麦或俄罗斯人群的情况相符。然而,据报道,纯合子45,X概念中只有1%是可存活的,这表明与X或Y染色体的嵌合是必要的。据了解,传统的带型分析对于区分TS的变异性质绝对必要。此外,分子遗传学或分子细胞遗传学研究可以确定嵌合的性质。本研究进一步表明常染色体参与导致青春期女孩性发育异常。

相似文献

1
X chromosomal abnormalities in Indian adolescent girls.印度青春期女孩的X染色体异常
Teratog Carcinog Mutagen. 2003;Suppl 1:245-53. doi: 10.1002/tcm.10052.
2
Laparoscopy in endocrine and genetic disorders of the gonads.腹腔镜检查在性腺内分泌和遗传性疾病中的应用。
Acta Endocrinol Suppl (Copenh). 1975;192:1-124.
3
Primary amenorrhoea in a patient with mosaicism for monosomy X and a derivative X-chromosome.一名患有X单体嵌合体和一条衍生X染色体的患者出现原发性闭经。
Genet Couns. 2010;21(3):335-42.
4
Cytogenetic studies in amenorrhea.闭经的细胞遗传学研究。
Saudi Med J. 2007 Feb;28(2):187-92.
5
Mosaic ring X chromosome in a case of secondary amenorrhea.一例继发性闭经患者的嵌合环形X染色体。
Fertil Steril. 2008 Oct;90(4):1198.e19-21. doi: 10.1016/j.fertnstert.2007.11.004. Epub 2008 Jan 4.
6
Cytogenetic study of primary amenorrhoea.原发性闭经的细胞遗传学研究。
J Indian Med Assoc. 1995 Aug;93(8):291-2.
7
[Screening for Y chromosome sequences in patients with Turner syndrome].[特纳综合征患者Y染色体序列筛查]
Acta Med Port. 2002 Mar-Apr;15(2):89-100.
8
Analysis of Turner syndrome patients within the Jordanian population, with a focus on four patients with Y chromosome abnormalities.分析约旦人群中的特纳综合征患者,重点关注四位存在 Y 染色体异常的患者。
Sex Dev. 2013;7(6):295-302. doi: 10.1159/000354279. Epub 2013 Aug 29.
9
Gonadoblastoma in Turner syndrome patients with nonmosaic 45,X karyotype and Y chromosome sequences.具有非嵌合型45,X核型和Y染色体序列的特纳综合征患者中的性腺母细胞瘤。
Cancer Genet Cytogenet. 2004 Apr 1;150(1):70-2. doi: 10.1016/j.cancergencyto.2003.08.011.
10
[Analysis of the small supernumerary marker chromosome in Turner syndrome with 45, X/46, X, + mar karyotype].[45,X/46,X,+mar核型特纳综合征中额外小标记染色体的分析]
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Aug;26(4):461-4.

引用本文的文献

1
Clinicoepidemiological Profile of Disorders of Sex Development Presenting to a Tertiary Care Center: A Descriptive Observational Study.三级医疗中心性发育障碍的临床流行病学概况:一项描述性观察研究。
J Indian Assoc Pediatr Surg. 2025 May-Jun;30(3):356-360. doi: 10.4103/jiaps.jiaps_252_24. Epub 2025 Mar 12.
2
Clinical profile and cytogenetic correlations in females with primary amenorrhea.原发性闭经女性的临床特征与细胞遗传学相关性
Clin Exp Reprod Med. 2023 Sep;50(3):192-199. doi: 10.5653/cerm.2023.05848. Epub 2023 Jun 13.
3
Etiological evaluation of adolescents with primary amenorrhea.
原发性闭经青少年的病因学评估。
Indian J Pediatr. 2014 Sep;81(9):861-5. doi: 10.1007/s12098-013-1266-6. Epub 2013 Nov 1.