Mark H F, Mendoza T, Abuelo D, Beauregard L J, May J B, LaMarche P H
J Med Genet. 1977 Jun;14(3):221-3. doi: 10.1136/jmg.14.3.221.
The birth of a child is described with Down syndrome followed by the conception of a fetus bearing the t(21q21q) chromosome in 100% of their cells in a women mosiac for the translocation in less than 10% of 2 of her examined tissues and in none of the cells in her peripheral blood. Various hypotheses for explaining the above findings are discussed. The importance of examining as many parental tissues as possible for the detection of low percentage mosiacism is stressed.
一名患有唐氏综合征的儿童出生,随后一名女性怀上了一个胎儿,该胎儿100%的细胞都携带t(21q21q)染色体,该女性是易位嵌合体,在所检查的2种组织中,检出率不到10%,而在外周血的细胞中未检出。文中讨论了解释上述发现的各种假说。强调了尽可能多地检查亲代组织对于检测低比例嵌合体的重要性。