Suppr超能文献

持续性苗勒管综合征伴睾丸横位异位及精子发生

Persistent müllerian duct syndrome with transverse testicular ectopia and spermatogenesis.

作者信息

Martin E L, Bennett A H, Cromie W J

机构信息

Division of Urological Surgery, Albany Medical Center Hospital, New York.

出版信息

J Urol. 1992 Jun;147(6):1615-7. doi: 10.1016/s0022-5347(17)37646-2.

Abstract

Normal male sexual differentiation is dependent on at least 2 factors: 1) testosterone and 2) müllerian inhibiting factor. The absence of müllerian inhibiting factor is responsible for a rare form of male pseudohermaphroditism, the persistent müllerian duct syndrome or hernia uteri inguinale. Patients with this syndrome present with persistent müllerian structures and the syndrome may be associated with transverse testicular ectopia. Additionally, most patients have azoospermia. We report a case of persistent müllerian duct syndrome with transverse testicular ectopia in which sperm are documented in the ejaculate.

摘要

正常男性性分化至少依赖于两个因素

1)睾酮和2)苗勒管抑制因子。苗勒管抑制因子的缺失导致一种罕见的男性假两性畸形,即持续性苗勒管综合征或腹股沟子宫疝。患有这种综合征的患者会出现持续性苗勒管结构,并且该综合征可能与睾丸横过异位有关。此外,大多数患者无精子症。我们报告一例伴有睾丸横过异位的持续性苗勒管综合征病例,该病例精液中存在精子。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验