Alves Cresio, Braid Zilda, Coeli Fernanda Borchers, Mello Maricilda Palandi de
Pediatric Endocrinology Service, Hospital Universitário Professor Edgard Santos, Faculty of Medicine, Universidade Federal da Bahia, Salvador, BA, Brazil.
Arq Bras Endocrinol Metabol. 2010 Nov;54(8):685-9. doi: 10.1590/s0004-27302010000800004.
The XX male syndrome - Testicular Disorder of Sexual Differentiation (DSD) is a rare condition characterized by a spectrum of clinical presentations, ranging from ambiguous to normal male genitalia. We report hormonal, molecular and cytogenetic evaluations of a boy presenting with this syndrome. Examination of the genitalia at age of 16 months, showed: penis of 3.5 cm, proximal hypospadia and scrotal testes. Pelvic ultrasound did not demonstrate Mullerian duct structures. Karyotype was 46,XX. Gonadotrophin stimulation test yielded insufficient testosterone production. Gonadal biopsy showed seminiferous tubules without evidence of Leydig cells. Molecular studies revealed that SRY and TSPY genes and also DYZ3 sequences were absent. In addition, the lack of deletions or duplications of SOX9, NR5A1, WNT4 and NROB1 regions was verified. The infant was heterozygous for all microsatellites at the 9p region, including DMRT1 gene, investigated. Only 10% of the patients are SRY-negative and usually they have ambiguous genitalia, as the aforementioned patient. The incomplete masculinization suggests gain of function mutation in one or more genes downstream to SRY gene.
XX男性综合征——性分化睾丸疾病(DSD)是一种罕见病症,其临床症状表现多样,从生殖器模糊到正常男性生殖器都有。我们报告了一名患有该综合征男孩的激素、分子和细胞遗传学评估情况。16个月大时对其生殖器进行检查,结果显示:阴茎长3.5厘米,近端尿道下裂,阴囊内有睾丸。盆腔超声未显示苗勒管结构。核型为46,XX。促性腺激素刺激试验显示睾酮分泌不足。性腺活检显示有生精小管,但未发现莱迪希细胞。分子研究表明,SRY和TSPY基因以及DYZ3序列均缺失。此外,还证实SOX9、NR5A1、WNT4和NROB1区域不存在缺失或重复。在所研究的包括DMRT1基因在内的9p区域的所有微卫星上,该婴儿均为杂合子。只有10%的患者SRY呈阴性,而且通常他们的生殖器模糊,就像上述患者一样。不完全男性化表明SRY基因下游的一个或多个基因发生了功能获得性突变。