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[正常男性表型或尿道下裂与女性核型。儿童及青少年的XX男性综合征]

[Normal male phenotype or hypospadias and female karyotype. XX male syndrome in children and adolescents].

作者信息

Naud C, Toublanc J E, Fellous M, Casanova M, Seboun E, Canlorbe P, Job J C

出版信息

Arch Fr Pediatr. 1985 Dec;42(10):835-8.

PMID:2870693
Abstract

A morphologically normal 46 XX karyotype has been found in 8 patients with male phenotype, either normal (3 cases) or hypospadiac (5 cases) studied at age 1 month to 15 years. Five had cryptorchidism. Pubertal follow-up was obtained in 6 patients and showed that they had hypogonadism with small testes, and a mean adult height of 163 cm. The hormonal investigations gave normal results before puberty, then after the onset of puberty a hypergonadotropic hypogonadism. Testicular biopsy showed alterations from age 8 years. Studies using Y-specific probes in 3 patients have shown the presence of Y genetic material in 2 and absence in 1, thus demonstrating genetic heterogeneity of the XX males.

摘要

在8例具有男性表型的患者中发现了形态正常的46 XX核型,这些患者年龄在1个月至15岁之间,表型正常(3例)或患有尿道下裂(5例)。5例有隐睾症。对6例患者进行了青春期随访,结果显示他们存在性腺功能减退,睾丸较小,成年平均身高为163厘米。激素检查在青春期前结果正常,青春期开始后出现高促性腺激素性性腺功能减退。睾丸活检显示8岁起就有改变。对3例患者使用Y特异性探针进行的研究表明,2例存在Y遗传物质,1例不存在,从而证明了XX男性的遗传异质性。

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