Van Buggenhout G J, Hamel B C, Trommelen J C, Mieloo H, Smeets D F
Department of Human Genetics, University Hospital Nijmegen, The Netherlands.
J Med Genet. 1994 Oct;31(10):807-10. doi: 10.1136/jmg.31.10.807.
We present a male patient with Down-Turner mosaicism (45,X/46,X,+21/47,XY,+21) and review 27 similar cases reported so far. Clinical features of Down's syndrome were present in all cases, whereas a combination of features of both Ullrich-Turner syndrome and Down's syndrome was reported in 61% of the patients. However, one has to bear in mind that several stigmata of Ullrich-Turner syndrome can also be present in patients with Down's syndrome and vice versa. In most of the patients two different cell lines were encountered, although cases with one, three, and even four different cell lines have been reported. Of 28 patients, 21 showed female external genitalia, four were phenotypically male, and three showed ambiguous genitalia. Only six patients (21%) carried a Y chromosome, which is far less than expected.
我们报告了一名患有唐氏-特纳嵌合体(45,X/46,X,+21/47,XY,+21)的男性患者,并回顾了迄今为止报道的27例类似病例。所有病例均有唐氏综合征的临床特征,而61%的患者同时具有乌尔里希-特纳综合征和唐氏综合征的特征组合。然而,必须记住,唐氏综合征患者也可能出现乌尔里希-特纳综合征的一些体征,反之亦然。在大多数患者中发现了两种不同的细胞系,尽管也有报道称存在一种、三种甚至四种不同细胞系的病例。28例患者中,21例表现为女性外生殖器,4例表型为男性,3例表现为生殖器模糊。只有6例患者(21%)携带Y染色体,这远低于预期。