Dessens Arianne B, Slijper Froukje M E, Drop Stenvert L S
Pediatrics Department, Division of Pediatric Endocrinology, Erasmus Medical Centre, Sophia Children's Hospital, Room SP-3435, POB 2060, 3000 CB, Rotterdam, The Netherlands.
Arch Sex Behav. 2005 Aug;34(4):389-97. doi: 10.1007/s10508-005-4338-5.
This article reviews the literature on studies and case reports on gender identity and gender identity problems, gender dysphoria, and gender change in chromosomal females with congenital adrenal hyperplasia, raised male or female. The large majority (94.8%) of the patients raised female (N= 250) later developed a gender identity as girls and women and did not feel gender dysphoric. But 13 (5.2%) patients had serious problems with their gender identity. This percentage is higher than the prevalence of female-to-male transsexuals in the general population of chromosomal females. Among patients raised male, serious gender identity problems were reported in 4 (12.1%) out of 33 patients. From these observations, we conclude that the assignment to the female gender as a general policy for 46,XX patients with CAH appears justified, even in severely masculinized 46,XX newborns with CAH (Prader stage IV or V).
本文综述了有关性别认同及性别认同问题、性别焦虑症,以及先天性肾上腺皮质增生症(CAH)的染色体核型为女性且自幼按男性或女性抚养的患者性别转变的研究及病例报告的文献。绝大多数(94.8%)自幼按女性抚养的患者(N = 250)后来形成了女性的性别认同,并未感到性别焦虑。但有13名(5.2%)患者存在严重的性别认同问题。这一比例高于染色体核型为女性的普通人群中女性向男性转变的易性症患者的患病率。在自幼按男性抚养的患者中,33名患者中有4名(12.1%)报告存在严重的性别认同问题。基于这些观察结果,我们得出结论,对于患有CAH的46,XX患者,即使是患有严重男性化表现的46,XX新生儿CAH(普拉德IV期或V期),将其按女性性别抚养作为一项通用政策似乎是合理的。