印度少女的X染色体异常。

Bani Bandana Ganguly, Sumedha Sahni
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引用次数: 10

摘要

在青春期的女孩中,原发性闭经是一个主要问题,通常被怀疑为特纳综合征(TS),两条X染色体中的一条完全或部分缺失。不能来月经的女孩主要由妇科医生在体格检查、骨盆超声检查、内分泌检查和细胞遗传学分析的帮助下进行调查。对来自全国不同地区的280例此类病例进行了染色体分析。采用外周血淋巴细胞培养标准方案进行中期染色体制备和g带染色体常规分析。共有29%的病例发现染色体异常,包括涉及性染色体的TS和睾丸女性化综合征。在性染色体异常的人群中,34%的表型女性有46、XY核型,51%的人有45、X系或嵌合系,X系有正常的XX或其他畸变。TS组的分类进一步表明,出现月经初潮缺席或延迟的印度少女的变异TS谱与比利时、丹麦或俄罗斯人群相符。然而,据报道,只有1%的纯45系,X受孕是可行的,这表明与X或Y染色体嵌合的必要性。传统的条带分析对于分离TS的变异性质是绝对必要的,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不正常。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
X chromosomal abnormalities in Indian adolescent girls.

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.

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