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46,XX性发育障碍男性:一例报告

46,XX male disorder of sexual development:a case report.

作者信息

Anık Ahmet, Çatlı Gönül, Abacı Ayhan, Böber Ece

机构信息

Dokuz Eylül University Faculty of Medicine, Department of Pediatric Endocrinology, İzmir, Turkey. E-mail:

出版信息

J Clin Res Pediatr Endocrinol. 2013;5(4):258-60. doi: 10.4274/Jcrpe.1098.

Abstract

The main factor influencing sex determination of an embryo is the sex-determining region Y (SRY), a master regulatory gene located on the Y chromosome. The presence of SRY causes the bipotential gonad to differentiate into a testis. However, some individuals carry a Y chromosome but are phenotypically female (46,XY females) or have a female karyotype but are phenotypically male (46,XX males). 46, XX male is rare (1:20 000 in newborn males), and SRY positivity is responsible for this condition in approximately 90% of these subjects. External genitalia of 46,XX SRY-positive males appear as normal male external genitalia, and such cases are diagnosed when they present with small testes and/or infertility after puberty. Herein, we report an adolescent who presented with low testicular volume and who was diagnosed as a 46,XX male. SRY positivity was demonstrated in the patient by fluorescence in situ hybridization method.

摘要

影响胚胎性别决定的主要因素是Y染色体性别决定区(SRY),这是一个位于Y染色体上的主要调控基因。SRY的存在会使双潜能性腺分化为睾丸。然而,一些个体虽携带Y染色体但表型为女性(46,XY女性),或具有女性核型但表型为男性(46,XX男性)。46,XX男性较为罕见(在新生男婴中的比例为1:20000),在这些患者中,约90%的病例是由SRY阳性导致的。46,XX SRY阳性男性的外生殖器表现为正常男性外生殖器,此类病例在青春期后出现睾丸小和/或不育时被诊断出来。在此,我们报告一名青春期男性,其睾丸体积小,被诊断为46,XX男性。通过荧光原位杂交法在该患者中证实了SRY阳性。

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