Costa T, Lambert M, Teshima I, Ray P N, Richer C L, Dallaire L
Department of Pediatrics, The Hospital for Sick Children, Toronto, Canada.
Am J Med Genet. 1998 Jan 6;75(1):40-4.
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.
我们报告了两组单卵双胞胎(MZTs),其出生时表型性别不一致,其中女性双胞胎有乌尔里希-特纳综合征的体征。对第一对双胞胎中的女性进行的细胞遗传学研究显示,淋巴细胞中有45,X/46,XY嵌合体,但从两个不同部位的皮肤活检以及性腺组织培养的成纤维细胞仅显示45,X细胞。男性在血液淋巴细胞和皮肤成纤维细胞中均显示嵌合体。在第二个家庭中,双胞胎在淋巴细胞中也均显示嵌合体。女性皮肤和性腺组织的成纤维细胞具有45,X核型,但与第一个家庭不同的是,男性双胞胎皮肤活检及输精管旁结缔组织的成纤维细胞具有正常男性核型。单卵双胞胎中表型性别不一致的情况很少见。与我们的病例一样,之前报道的9组MZTs均存在性染色体异常嵌合体。在孪生过程之前、伴随或之后导致Y染色体丢失的有丝分裂错误可以解释所报道的核型组合。