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46,XX真两性畸形患者及45,X混合型性腺发育不全患者中Y特异性DNA序列的缺失

Absence of Y-specific DNA sequences in human 46,XX true hermaphrodites and in 45,X mixed gonadal dysgenesis.

作者信息

Waibel F, Scherer G, Fraccaro M, Hustinx T W, Weissenbach J, Wieland J, Mayerová A, Back E, Wolf U

出版信息

Hum Genet. 1987 Aug;76(4):332-6. doi: 10.1007/BF00272440.

Abstract

A search for Y-specific DNA sequences has been performed in a sample of seven 46,XX true hermaphrodites and one 45,X mixed gonadal dysgenesis case and compared with a sample of 11 XX males. Using six Y-specific DNA probes no hybridization signal was obtained in the hermaphrodite group; in contrast, all XX males gave a positive signal with at least one probe. This difference is statistically highly significant. We conclude that the aetiology of true hermaphroditism is different from that of the XX male syndrome. As all cases of the hermaphrodite group are positive for the serological sex-specific antigen (Sxs) it is concluded that this antigen can be present even in the absence of Y-specific DNA.

摘要

在一个包含7例46,XX真两性畸形患者样本和1例45,X混合性性腺发育不全病例样本中进行了Y特异性DNA序列的搜索,并与11例XX男性样本进行了比较。使用6种Y特异性DNA探针,在两性畸形组中未获得杂交信号;相比之下,所有XX男性至少对一种探针给出阳性信号。这种差异在统计学上具有高度显著性。我们得出结论,真两性畸形的病因与XX男性综合征不同。由于两性畸形组的所有病例血清学性别特异性抗原(Sxs)均为阳性,因此得出结论,即使在没有Y特异性DNA的情况下,这种抗原也可能存在。

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