核型
生物
X染色体
特纳综合征
单卵双胞胎
结缔组织
Y染色体
皮肤活检
染色体
表型
性腺
遗传学
活检
内分泌学
内科学
医学
基因
作者
Teresa Costa,Marie Lambert,Ikuko Teshima,P N Ray,Claude‐Lise Richer,Louis Dallaire
出处
期刊:American journal of medical genetics
[Wiley]
日期:1998-01-06
卷期号:75 (1): 40-44
被引量:53
标识
DOI:10.1002/(sici)1096-8628(19980106)75:1<40::aid-ajmg9>3.0.co;2-u
摘要
We report on two sets of monozygotic twins (MZTs) discordant for phenotypic sex ascertained at birth when the female twin was noted to have signs of the Ullrich-Turner syndrome. Cytogenetic investigations on the female of the first pair showed 45,X/46,XY mosaicism in lymphocytes but fibroblasts grown from two skin biopsies at separate sites and from gonadal tissue showed only 45,X cells. The male showed mosaicism in both blood lymphocytes and skin fibroblasts. In the second family, both twins also showed mosaicism in lymphocytes. The female had a 45,X karyotype in fibroblasts from skin and gonadal tissue, but in contrast to the first family, the male twin had a normal male karyotype in fibroblasts from skin biopsy and from connective tissue adjacent to the vas deferens. Discordant phenotypic sex in monozygotic twins is rare. As in our cases, the nine previously reported sets of MZTs all had mosaicism for sex chromosome abnormalities. A mitotic error leading to the loss of a Y chromosome prior to, accompanying, or following the twinning process would account for the reported combinations of karyotypes. Am. J. Med. Genet. 75:40–44, 1998. © 1998 Wiley-Liss, Inc.
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