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唐氏综合征女孩的血液嵌合体和可能的雌雄同体效应导致 Müllerian 衍生物发育不良。

Blood chimerism in a girl with Down syndrome and possible freemartin effect leading to aplasia of the Müllerian derivatives.

机构信息

Institute of Human Genetics, ZMBE Westfalian Wilhelms-University of Münster and University Clinics Münster, Münster, Germany.

出版信息

Hum Reprod. 2010 May;25(5):1339-43. doi: 10.1093/humrep/deq048. Epub 2010 Feb 26.

Abstract

Cytogenetic and molecular genetic analysis in a case of sex-discordant dizygotic twins revealed blood chimerism in the girl (46,XY in blood and 47,XX, + 21 in fibroblasts) caused by feto-fetal transfusion from her healthy brother. The girl presented with Down syndrome, aplasia of the uterus and the Fallopian tubes and normal female external genitalia. We propose that the lack of Müllerian structures is caused by the effect of the Müllerian inhibiting substance transferred from the male to the female twin in early pregnancy. This disorder of sex development is known as freemartin phenomenon in female cattle from sex-discordant twin pairs.

摘要

在一例性不一致的双卵双胞胎中进行细胞遗传学和分子遗传学分析,发现女孩(血液为 46,XY,成纤维细胞为 47,XX,+21)存在血液嵌合体,这是由她健康的兄弟胎内输血引起的。该女孩患有唐氏综合征,子宫和输卵管发育不全,以及正常的女性外生殖器。我们提出,米勒管结构的缺失是由早孕时从男性向女性双胞胎传递的米勒管抑制物质引起的。这种性发育障碍在性不一致的双胎牛中被称为“雌雄同体现象”。

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