Donahoe P K, Crawford J D, Hendren W H
J Pediatr Surg. 1978 Jun;13(3):293-301. doi: 10.1016/s0022-3468(78)80403-5.
True hermaphroditism is a very rare form of ambiguous genitalia characterized by the presence of both ovarian and testicular tissue in the same individual. Sixty percent of these patients have a 46,XX karyotype; however, most have H-Y antigen detectable. Since H-Y antigen is thought to be the gene product of the short arm of the Y, then the short arm must be present somewhere in the karyotype. Products of the short arm loci are thought to initiate testicular differentiation and male determination. The long arm of the Y has not been detected in true hermaphrodites. Testicular histology in true hermaphrodites is characterized by spermatogenic arrest, causing us to speculate that the long arm of the Y might be essential for germ cell maturation beyond the spermatogonia state.
真两性畸形是一种极为罕见的两性生殖器模糊形式,其特征为同一个体中同时存在卵巢和睾丸组织。这些患者中有60%具有46,XX核型;然而,大多数患者可检测到H-Y抗原。由于H-Y抗原被认为是Y染色体短臂的基因产物,那么短臂必定存在于核型的某个位置。短臂基因座的产物被认为可启动睾丸分化和男性性别决定。在真两性畸形患者中未检测到Y染色体长臂。真两性畸形患者的睾丸组织学特征为生精停滞,这使我们推测Y染色体长臂可能对于精原细胞状态之后的生殖细胞成熟至关重要。