性发育障碍患者的生育问题管理。

Endocrine development Pub Date : 2014-01-01 Epub Date: 2014-09-09 DOI:10.1159/000363633
Gabriela Guercio, Rodolfo A Rey
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引用次数: 25

摘要

生育潜力是多学科团队在处理性别分配、手术管理、向患者及其家属披露的过程以及性发育障碍(DSD)患者的预期长期结果时应考虑的问题之一。在本文中,我们回顾了目前关于生殖潜能的证据:(1)发育不良的DSD,包括纯粹和部分性腺发育不良,性腺不对称分化,卵睾丸DSD和46xx睾丸DSD;(2) 46、XY型DSD是由于睾丸激素产生或作用异常引起的,包括睾酮产生不足、双氢睾酮缺乏、雄激素不敏感和抗勒氏激素或其受体缺陷;(3)46、XX型DSD是由于无睾丸组织的个体雄激素暴露过多引起的,即先天性肾上腺增生和芳香酶缺乏。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fertility issues in the management of patients with disorders of sex development.

Fertility potential is one of the issues that should be considered by the multidisciplinary team when addressing gender assignment, surgical management, the process of disclosure to patients and their families, and prospective long-term outcomes of individuals with disorders of sex development (DSD). In this article, we review the current evidence of the fertility potential of patients with: (1) dysgenetic DSD, including pure and partial gonadal dysgenesis, asymmetric gonadal differentiation, ovotesticular DSD and 46,XX testicular DSD; (2) 46,XY DSD due to abnormal testicular hormone production or action, including testosterone production deficiencies, dihydrotestosterone deficiency, androgen insensitivity and defects in anti-Müllerian hormone or its receptor, and (3) 46,XX DSD due to excessive androgen exposure in individuals with no testicular tissue, i.e. congenital adrenal hyperplasia and aromatase deficiency.

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