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[苗勒管结构抑制因子缺失。一例报告]

[Absence of the inhibitor factor of the Mullerian structures. Report of a case].

作者信息

Herrero Lugo A, Vasconcelos Ordaz V M, Castillo Castorena L E, Zonana Farca E, Rodríguez Rodríguez S

出版信息

Ginecol Obstet Mex. 1978 Dec;44(266):433-9.

PMID:33872
Abstract

A 30 year old patient with normal masculine phenotype, karyotype 46 XY with a congenital left inguinal hernia, was studied. This hernia contained (at surgery): uterus, tubes and a hypoplasic vagina, as well as testis. The Müllerian structures and the right testicle, were resected, and left orchidopexy was performed. FSH, LH, testosterone, prolactine, B-HCG in blood by radioimmunoanalysis, total estrogens, 17-ketosteroids and 17-hydroxicorticosteroids in urine, were all normal. Roentgenologic and endoscopic urologic studies were normal. A post-operative study of semen showed moderate oligospermia. The factors involved in masculine sexual differentiation, were reviewed, specially the inhibitory factor of Müllerian structures.

摘要

对一名30岁男性表型正常、核型为46 XY且患有先天性左侧腹股沟疝的患者进行了研究。该疝(手术时)包含:子宫、输卵管、发育不全的阴道以及睾丸。切除了苗勒管结构和右侧睾丸,并进行了左侧睾丸固定术。通过放射免疫分析测定血液中的促卵泡生成素(FSH)、促黄体生成素(LH)、睾酮、催乳素、β - 人绒毛膜促性腺激素(β - HCG),尿液中的总雌激素、17 - 酮类固醇和17 - 羟皮质类固醇,结果均正常。X线和内镜泌尿外科检查也正常。术后精液检查显示中度少精子症。对男性性别分化所涉及的因素进行了综述,特别关注了苗勒管结构的抑制因子。

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