Mejía-Baltodano G, Bobadilla L, Gonzalez R M, Barros-Núñez P
Division de Genética, Centro de Investigación Biomeédica de Occidente, Instituto Mexicano del Seguro Social, Guadalajara, Jalisco, Mexico.
Ann Genet. 1997;40(3):164-8.
We report a family in which the father carries a pericentric inversion involving two third of the chromosome 18 (p11.2q22). Of his three children, the proposita and her youngest brother show partial duplication of the short arm and partial deficiency of the long arm; the oldest sister shows the other recombinant (partial duplication of the long arm and partial deficiency of the short arm). In the literature, we found only one family in which both recombinants of a parental pericentric inversion were present in the same offspring and none with three affected and both kinds of recombinants. A review of the reported familial cases reveals that the risk of aneusomy of recombination, at least for chromosome-18 inversion carriers, may be close to 20% and no only 5-10% as previously reported.
我们报告了一个家系,其中父亲携带涉及18号染色体三分之二(p11.2q22)的臂间倒位。在他的三个孩子中,先证者及其最小的弟弟表现出短臂部分重复和长臂部分缺失;最大的姐姐表现出另一种重组类型(长臂部分重复和短臂部分缺失)。在文献中,我们仅发现一个家系,其中父母臂间倒位的两种重组类型出现在同一后代中,且没有一个家系中有三个孩子受影响且存在两种重组类型。对已报道的家族病例的回顾显示,重组体发生非整倍体的风险,至少对于18号染色体倒位携带者而言,可能接近20%,而并非如先前报道的仅为5-10%。