Rohatgi M, Menon P S, Verma I C, Iyengar J K
J Urol. 1987 Feb;137(2):263-7. doi: 10.1016/s0022-5347(17)43973-5.
We studied 20 patients with advanced degrees of hypospadias and undescended testes for the presence of an intersex disorder. A comprehensive clinical, cytogenetic, endocrinological and surgical evaluation was performed. All patients were found to have an intersex disorder, including 10 with male pseudohermaphroditism and 10 with a gonadal/genetic intersex disorder. In the latter group 4 patients had mixed gonadal dysgenesis, 3 had dysgenetic male pseudohermaphroditism, 1 had the 46XX male syndrome, 1 had true hermaphroditism and 1 had Klinefelter's syndrome. Genetic and gonadal intersex disorders were more frequent in patients with a unilateral undescended testis and perineal hypospadias.
我们研究了20例患有重度尿道下裂和隐睾的患者,以确定是否存在两性畸形障碍。进行了全面的临床、细胞遗传学、内分泌学和外科评估。所有患者均被发现患有两性畸形障碍,其中10例为男性假两性畸形,10例为性腺/基因性两性畸形障碍。在后一组中,4例患者患有混合性性腺发育不全,3例患有发育不全性男性假两性畸形,1例患有46XX男性综合征,1例患有真两性畸形,1例患有克兰费尔特综合征。基因性和性腺性两性畸形障碍在单侧隐睾和会阴型尿道下裂患者中更为常见。