46,XY性发育障碍伴女性外生殖器模糊1例报告

A. K. Sah, Bipin Maharjan, M. B. Adhikari, S. Baral, M. Giri
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引用次数: 0

摘要

性发育障碍(DSD)是一组在染色体、性腺或解剖水平上具有非典型性发育的先天性疾病。患有DSD的遗传性男性(46 XY DSD)可能表现为女性外生殖器表型、模糊或微阴茎。它是由子宫内不完全的男性化引起的,无论是否存在米勒结构。它要么是由于睾酮或DHT合成减少,要么是由于雄激素作用受损。在此,我们报告了一例13岁的女性儿童,其声音嘶哑,阴蒂逐渐增大,激素评估不提示5α还原酶缺乏、先天性肾上腺功能不全综合征或17β-羟基类固醇脱氢酶缺乏
本文章由计算机程序翻译,如有差异,请以英文原文为准。
46, XY Disorder of Sexual Development with Ambiguous Female External Genitalia: A Case Report
Disorder of Sexual Development (DSD) is a group of congenital conditions with atypical development of sex at chromosomal, gonadal or anatomic level. Genetic males with DSD (46 XY DSD) can present with female external genital phenotype, ambiguous, or a micropenis. It is caused by incomplete intrauterine masculinization with or without the presence of Müllerian structures. It results either from decreased synthesis of testosterone or DHT or from impairment of androgen action. Herein, we report a case of a 13-year child raised as female with hoarseness of voice and gradual enlargement of clitoris with hormonal assessment not suggestive of either 5 Alfa Reductase deficiency, Congenital Adrenal Insufficiency Syndrome or 17β-Hydroxysteroid Dehydrogenase deficiency
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