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巴布亚新几内亚一群患有5α-还原酶缺乏症的男性假两性畸形患者。

A cluster of male pseudohermaphrodites with 5 alpha-reductase deficiency in Papua New Guinea.

作者信息

Imperato-McGinley J, Miller M, Wilson J D, Peterson R E, Shackleton C, Gajdusek D C

机构信息

New York Hospital-Cornell University Medical Center, Department of Medicine, NY 10021.

出版信息

Clin Endocrinol (Oxf). 1991 Apr;34(4):293-8. doi: 10.1111/j.1365-2265.1991.tb03769.x.

Abstract

We report a cluster of male pseudohermaphrodites from the Simbari Anga linguistic group in the Eastern Highlands of Papua New Guinea. These subjects are born with a rudimentary clitoral-like penis and pseudovaginal perineoscrotal hypospadias. At puberty, the penis enlarges with concurrent growth of pubic and axillary hair and significant muscular development. There is significant facial hair, but it is less than that of their normal male siblings or other male relatives. Plasma collected from four adult subjects revealed elevated plasma testosterone levels, low to low normal dihydrotestosterone levels, and elevated testosterone/dihydrotestosterone ratios. All subjects had high urinary aetiocholanolone/androsterone ratios, and C19 and C21 5 beta/5 alpha metabolite ratios. Decreased 5 alpha-reductase activity was demonstrated in fibroblasts cultured from genital skin. The data indicate a phenotypic and biochemical profile similar to patients studied in the Dominican Republic, except for a greater abundance of facial and body hair. The phenotypic variability, as pertains to facial and body hair, may be related to differences in familial expression, as well as the degree of enzyme deficiency. Infants, thought to be females at birth, were reared as girls until puberty in a society practising one of the strictest gender segregations known. At puberty, these 'girls' were discovered to be boys, and a switch of gender roles was instituted. Recently, however, some Muniri, Dunkwi and northern Simbari hamlets recognize these individuals as male in infancy and rear them as boys, calling them 'kwalatmala' to distinguish them from normal males, accepting them as an intersex destined to occupy male adult roles.

摘要

我们报告了来自巴布亚新几内亚东部高地辛巴里·安加语族的一群男性假两性畸形患者。这些患者出生时阴茎类似阴蒂且发育不全,伴有会阴阴囊型尿道下裂和假阴道。青春期时,阴茎增大,同时阴毛和腋毛生长,肌肉显著发育。面部毛发较多,但比其正常男性同胞或其他男性亲属的少。从四名成年患者采集的血浆显示,血浆睾酮水平升高,双氢睾酮水平低至正常下限,睾酮/双氢睾酮比值升高。所有患者尿中本胆烷醇酮/雄酮比值以及C19和C21 5β/5α代谢物比值均升高。从生殖器皮肤培养的成纤维细胞中证实5α-还原酶活性降低。数据表明,除了面部和身体毛发更为浓密外,其表型和生化特征与在多米尼加共和国研究的患者相似。与面部和身体毛发相关的表型变异性可能与家族表达差异以及酶缺乏程度有关。在一个实行已知最严格性别隔离制度之一的社会中,这些出生时被认为是女性的婴儿一直被当作女孩抚养至青春期。然而,到了青春期,这些“女孩”被发现是男孩,于是性别角色发生了转变。不过,最近一些穆尼里、邓克维以及辛巴里北部的小村庄在婴儿期就将这些个体认定为男性并当作男孩抚养,称他们为“夸拉特马拉”,以将他们与正常男性区分开来,将他们当作注定要承担男性成年角色的双性人接纳。

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