Voelckel M A, Pellissier M C, Piquet C, N'Guyen C, Boccaccio I, Philip N, Mattei J F
INSERM, Unité 242, Centre de Génétique Médicale, Hôpital d'Enfants de la Timone, Marseille, France.
Am J Med Genet. 1991 Feb-Mar;38(2-3):374-7. doi: 10.1002/ajmg.1320380243.
We report on a large family (4 generations), with 77 studied individuals, 9 mentally retarded males, and one affected female with fragile X syndrome [fra(X)]. The analysis of 6 flanking polymorphic DNA markers showed that the affection is transmitted, through the carrier daughters to the grandsons and the greatgrandsons and that the great-grandfather is a transmitting male. This observation led us to question the importance of these clinically normal males, who are nonexpressing carriers and termed transmitting males. One propositus, described as a mentally retarded young man, had inherited identical restriction polymorphisms from his mother. Chromosome analysis showed a Klinefelter syndrome, with a fragile site in 18% of the cells leading to the conclusion that the nondisjunction occurred at the first stage of the maternal meiosis.
我们报告了一个大家庭(4代人),其中有77名被研究个体,9名智力发育迟缓男性,以及1名患有脆性X综合征[fra(X)]的患病女性。对6个侧翼多态性DNA标记的分析表明,这种病症通过携带致病基因的女儿传递给孙子和曾孙,且曾祖父是一名传递男性。这一观察结果让我们质疑这些临床正常男性的重要性,他们是无表达的携带者,被称为传递男性。一名被描述为智力发育迟缓的年轻人先证者,从他母亲那里继承了相同的限制性多态性。染色体分析显示为克兰费尔特综合征,18%的细胞中有一个脆性位点,由此得出结论,不分离发生在母本减数分裂的第一阶段。