Andersen O, Lundsteen C, Niebuhr E
Cytogenet Cell Genet. 1981;30(1):3-10. doi: 10.1159/000131581.
A complex four-break rearrangement between chromosomes 4 and 13 was ascertained in a 10-year-old mentally retarded girl. The rearrangement was inherited from the phenotypically normal mother, who had an inverted insertion of part of the long arm of chromosome 4 into the long arm of 13 and, in addition, a pericentric inversion of the deleted 4. Meiotic crossing-over between the normal and the inverted 4 resulted in a recombinant chromosome 4, which was inherited by the proband, together with the 13/4 insertion. In this way the proband became monosomic for 4q35 leads to qter and trisomic for 4pter leads to 4p15, but she showed only minor physical malformations, as compared with other reports on the trisomy 4p syndrome. The cytogenetic findings are difficult to describe using the ISCN nomenclature.
在一名10岁智力发育迟缓女孩中确定了4号和13号染色体之间复杂的四重断裂重排。这种重排遗传自表型正常的母亲,她的4号染色体长臂的一部分反向插入到13号染色体长臂中,此外,缺失的4号染色体发生了臂间倒位。正常4号染色体与倒位4号染色体之间的减数分裂交叉导致了一条重组4号染色体,先证者继承了这条重组4号染色体以及13/4插入。通过这种方式,先证者4号染色体q35至qter区段单体性,4号染色体pter至4p15区段三体性,但与其他关于4号染色体短臂三体综合征的报道相比,她仅表现出轻微的身体畸形。使用国际人类细胞遗传学命名法(ISCN)很难描述这些细胞遗传学发现。