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印度两性畸形患者的病因、临床特征、性别认同及长期随访

Etiology, clinical profile, gender identity and long-term follow up of patients with ambiguous genitalia in India.

作者信息

Ammini A C, Gupta R, Kapoor A, Karak A, Kriplani A, Gupta D K, Kucheria K

机构信息

Department of Endocrinology, All India Institute of Medical Sciences, New Delhi.

出版信息

J Pediatr Endocrinol Metab. 2002 Apr;15(4):423-30. doi: 10.1515/jpem.2002.15.4.423.

Abstract

There is little information on the profile of children with ambiguous genitalia in India. Presented here is an analysis of patients with ambiguous genitalia registered in a general endocrine clinic during the last 2 decades. Seventy-four patients (age 4 months to 36 years) were registered during this period. Fifty-two were more than 5 years old at the time of registration. Thirty-five were reared as females, 29 as males; nine children (4 months to 1 year old) were brought for sex assignment, and one (with epispadias) was brought for correction of urinary incontinence. Investigations revealed 28 patients with congenital adrenal hyperplasia, 14 dysgenetic male pseudohermaphroditism, ten true hermaphroditism, six partial androgen insensitivity, four castration and one epispadias. There were eight patients with perineal hypospadias with normal Leydig cell reserve (normal LH, FSH and testosterone response to LHRH). Sex of rearing and gender identity were concordant in all except the patients with perineal hypospadias with normal Leydig cell response. These observations support the theory that prenatal androgen exposure masculinizes the brain.

摘要

关于印度两性生殖器模糊儿童的情况,相关信息很少。本文呈现的是对过去20年在一家普通内分泌诊所登记的两性生殖器模糊患者的分析。在此期间登记了74名患者(年龄4个月至36岁)。登记时52名患者年龄超过5岁。35名患者被当作女性抚养,29名被当作男性抚养;9名儿童(4个月至1岁)前来进行性别指定,1名(患有尿道上裂)前来治疗尿失禁。检查发现28名患者患有先天性肾上腺皮质增生症,14名患有发育不全的男性假两性畸形,10名患有真两性畸形,6名患有部分雄激素不敏感,4名患有去势,1名患有尿道上裂。有8名患有会阴型尿道下裂且睾丸间质细胞储备正常(对促性腺激素释放激素的促黄体生成素、促卵泡生成素和睾酮反应正常)的患者。除了会阴型尿道下裂且睾丸间质细胞反应正常的患者外,抚养性别和性别认同在所有患者中都是一致的。这些观察结果支持产前雄激素暴露使大脑男性化这一理论。

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