Suppr超能文献

原发性闭经的细胞遗传学研究。

Cytogenetic study of primary amenorrhoea.

作者信息

Roy A K, Banerjee D

机构信息

Demonstrator of Pathology, Medical College, Calcutta.

出版信息

J Indian Med Assoc. 1995 Aug;93(8):291-2.

PMID:8713239
Abstract

A study of chromosomal pattern was done in 60 cases of primary amenorrhoea of different age groups to determine the incidences of chromosomal abnormalities in them and to detect those cases of classical 45, X Turner's syndrome and Turner mosaics that do not bear the Turner stigmata. Buccal smears were examined for sex chromatin followed by karyotype using leucocyte culture method. Majority (63.3%) of cases were found chromosomally incompetent of which the major abnormality was 45, X/46, XX mosaicism (33.3%) followed by 45, X Turner's syndrome (26.6%). But only 43.7% of these Turner's syndrome had classical Turner stigmata. Two cases of complete testicular feminisation syndrome with male genotype (46,XY) and inguinal testis were also detected.

摘要

对60例不同年龄组的原发性闭经患者进行了染色体模式研究,以确定其中染色体异常的发生率,并检测那些不具有特纳综合征体征的典型45,X特纳综合征和特纳嵌合体病例。先检查口腔涂片的性染色质,然后采用白细胞培养法进行核型分析。大多数(63.3%)病例被发现染色体异常,其中主要异常为45,X/46,XX嵌合体(33.3%),其次是45,X特纳综合征(26.6%)。但这些特纳综合征患者中只有43.7%具有典型的特纳综合征体征。还检测到2例具有男性基因型(46,XY)和腹股沟睾丸的完全性睾丸女性化综合征病例。

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