Piccione Maria, Maresi Emiliano, Zollino Marcella, Sanfilippo Cinzia, Seminara Laura, Neri Giovanni, Corsello Giovanni
U. O. Pediatria e Terapia Intensiva Neonatale, Dipartimento Materno Infantile, Università degli Studi di Palermo, Palermo, Italy.
Am J Med Genet A. 2008 Oct 15;146A(20):2681-7. doi: 10.1002/ajmg.a.32514.
Translocations involving the short arms of the X and Y chromosomes are uncommon and are often associated with anomalies in gonadal development. Segmental duplications of the X chromosome interfere with the formation of the testis in patients with a 46,XY karyotype. The gene products located within the duplicated segment, when present in double dose, may affect on male sex development. We report on a fetus with karyotype 46,XY,der (14)t(X;14) (p10;p10)dn. Attached to chromosome 14 is the entire short arm of the X chromosome. Therefore, the fetus is affected with a disomy of Xp, resulting in complete male to female sex reversal, as well as other structural defects. To the best of our knowledge, this is the first description of an XY fetus with a pure duplication of the entire short arm of X chromosome.
涉及X和Y染色体短臂的易位并不常见,且常与性腺发育异常相关。X染色体的节段性重复会干扰46,XY核型患者睾丸的形成。位于重复节段内的基因产物,若以双倍剂量存在,可能会影响男性性发育。我们报告了一例核型为46,XY,der(14)t(X;14)(p10;p10)dn的胎儿。附着于14号染色体的是X染色体的整个短臂。因此,该胎儿存在Xp双体,导致完全性的男性向女性性别反转,以及其他结构缺陷。据我们所知,这是首例关于X染色体整个短臂纯重复的XY胎儿的描述。