Ganguly Bani Bandana, Sahni Sumedha
Cytogenetics Division, Clinical Reference Laboratories, SRL Ranbaxy Ltd., Mumbai, India.
Teratog Carcinog Mutagen. 2003;Suppl 1:245-53. doi: 10.1002/tcm.10052.
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.
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。