Meyer-Bahlburg H F, Gruen R S, New M I, Bell J J, Morishima A, Shimshi M, Bueno Y, Vargas I, Baker S W
New York State Psychiatric Institute, New York 10032, USA.
Horm Behav. 1996 Dec;30(4):319-32. doi: 10.1006/hbeh.1996.0039.
The psychoendocrinology of the development of normal gender identity and its variations is poorly understood. Studies of gender development in individuals born with endocrinologically well-characterized intersex conditions are heuristically valuable for the disaggregation of factors that are acting in concert during normal development. Four 46,XX individuals with classical congenital adrenal hyperplasia (CAH) and atypical gender identity entered a comprehensive research protocol including systematic interviews and self-report inventories on gender role behavior and identity, sexual history, and psychiatric history. Some of the data on gender variables were compared to data from 12 CAH women with the salt-wasting variant (CAH-SW) with female gender identity. The four patients (ages 28, 35, 38, and 30 years) represented three different subtypes of classical early-onset CAH: 21-OH deficiency, simple virilizing (CAH-SV); 21-OH deficiency, salt-wasting (CAH-SW); and 11-beta-OH deficiency. Their medical histories were characterized by delay beyond infancy or lack of surgical feminization of the external genitalia and progressive virilization with inconsistent or absent glucocorticoid replacement therapy. Although three patients had undergone one or more genital surgeries, all had retained at least some orgasmic capacity. In regard to childhood gender-role behavior, the four gender-change patients tended to be more masculine or less feminine than (behaviorally masculinized) CAH-SW controls. All patients were sexually attracted to females only. The process of gender change was gradual and extended well into adulthood. The most plausible factors contributing to cross-gender identity development in these patients appeared to be neither a particular genotype or endocrinotype nor a sex-typing bias on the part of the parents but a combination of a gender-atypical behavioral self-image, a gender-atypical body image, and the development of erotic attraction to women. Implications for psychosocial management are also discussed.
正常性别认同发展及其变异的心理内分泌学仍未得到充分理解。对患有内分泌特征明确的两性畸形疾病个体的性别发展研究,对于剖析正常发育过程中协同作用的因素具有启发价值。四名患有经典型先天性肾上腺皮质增生症(CAH)且具有非典型性别认同的46,XX个体,进入了一项全面的研究方案,该方案包括关于性别角色行为和认同、性史以及精神病史的系统访谈和自我报告清单。将部分关于性别变量的数据与12名具有失盐型变异(CAH-SW)且具有女性性别认同的CAH女性的数据进行了比较。这四名患者(年龄分别为28岁、35岁、38岁和30岁)代表了经典早发型CAH的三种不同亚型:21-羟化酶缺乏症,单纯男性化型(CAH-SV);21-羟化酶缺乏症,失盐型(CAH-SW);以及11-β-羟化酶缺乏症。他们的病史特征为婴儿期后出现延迟或外生殖器未进行手术女性化,以及在糖皮质激素替代治疗不一致或未进行治疗的情况下出现渐进性男性化。尽管三名患者接受了一次或多次生殖器手术,但所有人都至少保留了一定的性高潮能力。关于儿童性别角色行为,这四名性别转变患者相较于(行为男性化的)CAH-SW对照组,往往更具男性化特征或更少女性化特征。所有患者仅被女性吸引。性别转变过程是渐进的,且一直持续到成年期。在这些患者中,导致跨性别认同发展的最合理因素似乎既不是特定的基因型或内分泌类型,也不是父母一方的性别类型偏见,而是性别非典型的行为自我形象、性别非典型的身体形象以及对女性产生的性吸引力的发展。文中还讨论了对心理社会管理的启示。