首页> 外文期刊>Archives of sexual behavior >Gender Identity and Sexual Function in 46,XX Patients with Congenital Adrenal Hyperplasia Raised as Males
【24h】

Gender Identity and Sexual Function in 46,XX Patients with Congenital Adrenal Hyperplasia Raised as Males

机译:在46中的性别同一性和性功能,XX患者患有先天性肾上腺增生的患者

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

In individuals with congenital adrenal hyperplasia (CAH) and 46,XX karyotype, androgens produced by the adrenal glands during the intrauterine development promote virilization of the genitals, which may even result in the development of a well-formed penis. Some of these children with late diagnosis are registered as males after birth. After obtaining approval from the internal review board, we evaluated gender identity and sexual function in four 46,XX severely virilized patients with CAH, who were originally registered and raised as males, assisted in our Disorders of Sexual Development Clinic. The evaluation consisted of questionnaires to assess gender identity and sexual activity and interview with the multidisciplinary team that provides care for these patients. The patients underwent surgery to remove uterus, ovaries, and remaining vaginal structures, in addition to implantation of testicular prosthesis and correction of hypospadias, when necessary. All four patients have developed a clear male gender identity, and when evaluated for sexual activity, they have reported having erections, libido, orgasms, and sexual attraction to women only. Two of these 4 patients had satisfactory sexual intercourses when assessed using the International Index of Erectile Function questionnaire. The other two patients who never had sexual intercourse reported not having a partner for sexual activity; one is 18 years old, and the other is 14 years old. This study showed that this group of 46,XX severely virilized patients with CAH, registered and raised as males, adapted well to the assigned male gender, with satisfactory sexual function in patients who had sexual intercourse.
机译:在具有先天性肾上腺增生(CAH)和46,XX核型的个体中,在宫内发育过程中由肾上腺产生的雄激素促进了生殖器的病毒,甚至可能导致形成良好的阴茎。这些患儿的一些患儿在出生后被注册为雄性。从内部审查委员会获得批准后,我们​​评估了四个46,XX严重有毒的CAH的性别身份和性功能,他最初注册并筹集为男性,辅助我们的性发展诊所。评估由调查问卷组成,以评估性别认同和性活动以及对提供这些患者提供护理的多学科团队的访谈。除了植入睾丸假体和恢复尿道痉挛的必要时,患者接受手术以除去子宫,卵巢和剩余的阴道结构。所有四名患者都制定了明确的男性性别身份,并且在评估性活动时,他们据报道,只有勃起,性欲,高潮和妇女的性吸引力。在评估使用国际勃起函数问卷调查问卷的评估时,这4名患者中有两名令人满意的性互生。另外两名从未有过性交的患者报告没有有性活动的伴侣;一个是18岁,另一个是14岁。本研究表明,该组46,XX严重有毒的CAH患者,注册并募集为雄性,适应分配的男性性别,具有性交性交的患者的令人满意的性功能。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号