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男性假两性畸形患儿:内分泌与代谢研究

Children with male pseudohermaphroditism: endocrine and metabolic studies.

作者信息

Saez J M, Frederich A, De Peretti E, Bertrand J

出版信息

Birth Defects Orig Artic Ser. 1971 May;7(6):150-8.

PMID:4281322
Abstract

In 22 children with male pseudohermaphroditism, plasma concentrations of testosterone and dehydroandrosterone sulfate were measured before and after HCG stimulation. In ten of them, nitrogen retention was measured both before and during treatment with testosterone-propionate. The results of this investigation allow the patients to be classified in the following groups 1) nine in which both the testicular function and the end-organ sensitivity to androgens were normal; 2) nine patients had an abnormal testicular function; 3) four patients had the testicular feminization syndrome. In addition, in one adolescent patient with familial male pseudohermaphroditism and gynecomastia, the pattern of plasma androgens under basal conditions, after HCG and following gonadectomy, suggest that the patient had an incomplete 17-ketosteroid reductase defect.

摘要

对22例男性假两性畸形患儿,在人绒毛膜促性腺激素(HCG)刺激前后测定了血浆睾酮和硫酸脱氢表雄酮浓度。其中10例在丙酸睾酮治疗前及治疗期间测定了氮潴留情况。本研究结果可将患者分为以下几组:1)9例睾丸功能及终末器官对雄激素的敏感性均正常;2)9例睾丸功能异常;3)4例患有睾丸女性化综合征。此外,在1例患有家族性男性假两性畸形和男子女性型乳房的青少年患者中,基础状态下、HCG刺激后及性腺切除后的血浆雄激素模式表明该患者存在不完全性17 - 酮类固醇还原酶缺陷。

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