Zenteno J C, López M, Vera C, Méndez J P, Kofman-Alfaro S
Servicio de Genética, Hospital General de México-Facultad de Medicina, UNAM, México, D. F., México.
Hum Genet. 1997 Oct;100(5-6):606-10. doi: 10.1007/s004390050561.
We report a Mexican family in which two sibs were identified as "classic" XX males without genital ambiguities. Molecular studies revealed that both patients were negative for several Y sequences, including SRY. A review of familial cases disclosed that this is the first family where a complete male phenotype was observed in Y-negative XX male non-twin brothers. These data suggest that an inherited loss-of-function mutation, in a gene participating in the sex-determining cascade, can induce normal male sexual differentiation in the absence of SRY.
我们报告了一个墨西哥家庭,其中两名同胞被鉴定为无生殖器模糊的“典型”XX男性。分子研究显示,两名患者的几个Y序列(包括SRY)均为阴性。对家族病例的回顾发现,这是首个在Y阴性的XX男性非双胞胎兄弟中观察到完全男性表型的家庭。这些数据表明,参与性别决定级联反应的基因中发生的遗传性功能丧失突变,在没有SRY的情况下也可诱导正常的男性性分化。