Walker A P, Bocian M
Am J Med Genet. 1987 May;27(1):3-22. doi: 10.1002/ajmg.1320270103.
We report on two sibs with duplication of the segment 8q12----8q21.2 resulting from malsegregation of a maternal insertional translocation: [inv ins (5;8)(p13;q12q21.2)]. The mother also carries a reciprocal translocation [t(1;6)(q31;q5)], which was transmitted in the balanced state to the propositi and to a phenotypically normal son and daughter. The literature on two translocations occurring in one individual and on insertional rearrangements is reviewed in terms of reproductive risks to balanced carriers. The two affected infants have a previously undescribed partial duplication of an interstitial segment of 8q and a pattern of abnormalities distinct from those seen in other partial duplications of 8. These infants are reviewed with 78 other cases of partial duplications of chromosome 8 with regard to phenotype-karyotype correlations.
我们报告了两例因母亲插入性易位错分离而导致8q12----8q21.2片段重复的同胞:[inv ins(5;8)(p13;q12q21.2)]。母亲还携带一个相互易位[t(1;6)(q31;q5)],该易位以平衡状态传递给先证者以及一个表型正常的儿子和女儿。本文从平衡携带者的生殖风险方面,对一个个体中发生的两种易位以及插入重排的文献进行了综述。这两名受影响的婴儿存在先前未描述的8q间质片段部分重复,且异常模式与其他8号染色体部分重复所见不同。本文结合其他78例8号染色体部分重复病例,对这些婴儿的表型-核型相关性进行了综述。