Casas-Vargas Andrea, Galvis Johanna, Blanco Jenny, Rengifo Laura, Usaquén William, Velasco Harvy
Grupo de Genética de Poblaciones e Identificación, Instituto de Genética, Universidad Nacional de Colombia, Bogotá, D.C., Colombia.
Biomedica. 2019 Dec 1;39(4):622-630. doi: 10.7705/biomedica.4687.
In most cases, male sexual differentiation occurs with SRY gene mediation. However, exceptional genotypes have been identified, as shown in this paper. This was a male adult patient seen at the Servicio de Paternidades, Instituto de Genética, Universidad Nacional de Colombia. The following procedures were carried out: Amelogenin gene and short tandem repeat analyses using human identification commercial kits, conventional karyotype, SRY fluorescent in situ hybridization, PCR analysis for Y chromosome microdeletions, clinical evaluation, and genetic counseling. We present an adult male with unambiguous genitalia, karyotype 46,XX, and an SRY negative and ZFY positive molecular profile. The diagnosis of nonsyndromic 46,XX testicular disorder of sex development (DSD) -a rare genetic condition- was established. Only 20 % of similarly diagnosed patients are SRY negative and exhibit diverse molecular profiles. Until now, available evidence seems to indicate that, even in the absence of SRY, the ZFY factor is involved in male sexual differentiation.
在大多数情况下,男性性分化是在SRY基因介导下发生的。然而,如本文所示,已鉴定出特殊的基因型。这是一名成年男性患者,在哥伦比亚国立大学遗传学研究所亲子鉴定服务处就诊。进行了以下检查:使用人类身份鉴定商用试剂盒进行牙釉蛋白基因和短串联重复序列分析、常规核型分析、SRY荧光原位杂交、Y染色体微缺失的PCR分析、临床评估和遗传咨询。我们报告一名成年男性,其生殖器明确,核型为46,XX,SRY阴性且ZFY阳性分子谱。确诊为非综合征性46,XX性发育障碍(DSD)——一种罕见的遗传疾病。在类似诊断的患者中,只有20%为SRY阴性且表现出不同的分子谱。到目前为止,现有证据似乎表明,即使没有SRY,ZFY因子也参与男性性分化。