Werner W, John B, Tuschy U, Knorr B, Herrmann F H
Zentralbl Gynakol. 1985;107(5):265-79.
Three female patients with Turner-syndrome (sexual infantilism, short stature and somatic Turner-stigmata) have been analysed cytogenetically by means of different banding techniques. A deletion of the distal heterochromatic band Yq12 of the Y chromosome was observed in a mosaic with a 45,X-cell line, i.e. the karyotype is 45,X/46,X,del(Y)(q12). In order to get information about the phenotypic expression of the 45,X/46,X,del(Yq) mosaicism all previously published cases have been reviewed. Comparing the phenotypes of all 45,X/46,X,del(Yq) mosaic cases three different phenotype categories of sexual development can be distinguished: female individuals with sexual infantilism and Turner-stigmata, individuals with ambiguous genitals, ranging from clitoris hypertrophy of female genitals to hypospadia of males, male individuals, who are infertile (azoospermic). A comparison of the appearance of external genitals with the status of gonads of all patients revealed an unequivocal relationship between the gonad status and the resulting phenotype category. Furthermore, the role of Y-chromosomal loci determining testicular differentiation (biological function of H-Y antigen) for male development has been emphasized. The effect of the 45,X-cell line on the expression of short stature and somatic Turner-stigmata is independent of sexual development. Considering the great phenotypic variability of the 45,X/46,X,del(Yq) mosaicism it seems impossible to deduce a definitive phenotype. This problem is acute in prenatal diagnosis especially.
对三名患有特纳综合征(性幼稚、身材矮小和躯体特纳体征)的女性患者采用不同的显带技术进行了细胞遗传学分析。在一个含有45,X细胞系的嵌合体中观察到Y染色体远端异染色质带Yq12缺失,即核型为45,X/46,X,del(Y)(q12)。为了获取有关45,X/46,X,del(Yq)嵌合体表型表达的信息,对所有先前发表的病例进行了回顾。比较所有45,X/46,X,del(Yq)嵌合病例的表型,可以区分出三种不同的性发育表型类别:患有性幼稚和特纳体征的女性个体、生殖器模糊的个体(从女性生殖器阴蒂肥大到男性尿道下裂)、不育(无精子症)的男性个体。对所有患者的外生殖器外观与性腺状态进行比较,发现性腺状态与最终表型类别之间存在明确的关系。此外,强调了Y染色体上决定睾丸分化的基因座(H-Y抗原的生物学功能)对男性发育的作用。45,X细胞系对身材矮小和躯体特纳体征表达的影响与性发育无关。考虑到45,X/46,X,del(Yq)嵌合体巨大的表型变异性,似乎无法推断出明确的表型。这个问题在产前诊断中尤为突出。