Joseph Angela Ann, Shabir Iram, Marumadi Eunice, Dada Reema, Ammini Ariachery C, Mehta Manju
J Pediatr Endocrinol Metab. 2013;26(9-10):915-20. doi: 10.1515/jpem-2013-0154.
There are few reports of adults with disorders of sexual development (DSD). Here we describe the clinical profile and results of psychological assessment of three siblings with 46, XY DSD caused by partial androgen insensitivity syndrome (PAIS). The elder sibling (aged 22 years) was reared as female, while the middle and youngest siblings (17 and 18 years of age), were reared as males. The gender identity was concordant with the sex of rearing. There was no gender dysphoria. The psychological distress that our patients experienced was due to the limitations placed on them by their medical condition. It did not permit them to experience various facets of being either male or female completely. The younger siblings reared as males had additional problems of gynecomastia and lack of male secondary sexual development.
关于成年性发育障碍(DSD)患者的报道较少。在此,我们描述了三名因部分雄激素不敏感综合征(PAIS)导致46, XY DSD的兄弟姐妹的临床特征及心理评估结果。年长的兄弟姐妹(22岁)被当作女性抚养,而中间和最小的兄弟姐妹(分别为17岁和18岁)被当作男性抚养。性别认同与抚养性别一致。没有性别焦虑症。我们的患者所经历的心理困扰是由于其身体状况给他们带来的限制。这使他们无法完全体验作为男性或女性的各个方面。被当作男性抚养的较年轻的兄弟姐妹还有乳腺增生和缺乏男性第二性征发育的额外问题。