Naito Katsusuke
Department of Urology, Yamaguchi University School of Medicine.
Nihon Rinsho. 2004 Feb;62(2):300-4.
True hermaphroditism in humans is defined as the simultaneous presence of both testicular and ovarian tissue in a single individual. I reviewed clinical findings, karyotype, findings of recent molecular analysis, diagnostic tools and treatment of true hermaphroditism. Recent molecular analysis in true hermaphroditism revealed that duplication of 22q was recognized in a 46,XX SRY-negative case. A 46,XX true hermaphrodite in which SRY was negative in blood leukocytes and epithelial oral cells but present and partially deleted in DNA obtained from the testicular portion of the ovotestes was reported. And also, the study using PCR and FISH analyses revealed the presence of hidden mosaicism for SRY or other Y sequences in some patients with XX true hermaphroditism and mosaicism for SRY limited to the gonads is an alternative mechanism for testicular development in 46,XX true hermaphrodites.
人类真性两性畸形的定义是在同一个体中同时存在睾丸组织和卵巢组织。我回顾了真性两性畸形的临床发现、核型、近期分子分析结果、诊断工具及治疗方法。真性两性畸形的近期分子分析显示,在一例46,XX SRY阴性病例中发现了22q重复。有报道称,一名46,XX真性两性畸形患者,其血液白细胞和口腔上皮细胞中的SRY为阴性,但从卵睾的睾丸部分获得的DNA中SRY呈阳性且部分缺失。此外,一项使用聚合酶链反应(PCR)和荧光原位杂交(FISH)分析的研究显示,一些XX真性两性畸形患者存在SRY或其他Y序列的隐匿性嵌合体,而SRY仅限于性腺的嵌合体是46,XX真性两性畸形患者睾丸发育的另一种机制。