Kartapradja Hannie, Marzuki Nanis Sacharina, Pertile Mark D, Francis David, Suciati Lita Putri, Anggaratri Helena Woro, Ambarwati Debby Dwi, Idris Firman Prathama, Lesmana Harry, Trimarsanto Hidayat, Paramayuda Chrysantine, Harahap Alida Roswita
Eijkman Institute for Molecular Biology, Jl. Diponegoro 69, Jakarta 10430, Indonesia.
Victorian Clinical Genetics Services (VCGS), Royal Children's Hospital, Flemington Road, Melbourne, VIC 3052, Australia.
Case Rep Genet. 2015;2015:321014. doi: 10.1155/2015/321014. Epub 2015 Feb 3.
We report an exceptional complex chromosomal rearrangement (CCR) found in three individuals in a family that involves 4 chromosomes with 5 breakpoints. The CCR was ascertained in a phenotypically abnormal newborn with additional chromosomal material on the short arm of chromosome 4. Maternal karyotyping indicated that the mother carried an apparently balanced CCR involving chromosomes 4, 6, 11, and 18. Maternal transmission of the derivative chromosome 4 resulted in partial trisomy for chromosomes 6q and 18q and a partial monosomy of chromosome 4p in the proband. Further family studies found that the maternal grandmother carried the same apparently balanced CCR as the proband's mother, which was confirmed using the whole chromosome painting (WCP) FISH. High resolution whole genome microarray analysis of DNA from the proband's mother found no evidence for copy number imbalance in the vicinity of the CCR translocation breakpoints, or elsewhere in the genome, providing evidence that the mother's and grandmother's CCRs were balanced at a molecular level. This structural rearrangement can be categorized as an exceptional CCR due to its complexity and is a rare example of an exceptional CCR being transmitted in balanced and/or unbalanced form across three generations.
我们报告了在一个家族的三名个体中发现的一种罕见的复杂染色体重排(CCR),该重排涉及4条染色体和5个断点。CCR是在一名表型异常的新生儿中确定的,其4号染色体短臂上有额外的染色体物质。母亲的核型分析表明,母亲携带一种明显平衡的CCR,涉及4号、6号、11号和18号染色体。衍生4号染色体的母系遗传导致先证者6号染色体长臂和18号染色体长臂部分三体以及4号染色体短臂部分单体。进一步的家族研究发现,外祖母携带与先证者母亲相同的明显平衡的CCR,这通过全染色体涂染(WCP)荧光原位杂交得到证实。对先证者母亲的DNA进行高分辨率全基因组微阵列分析,未发现CCR易位断点附近或基因组其他位置存在拷贝数失衡的证据,这表明母亲和外祖母的CCR在分子水平上是平衡的。这种结构重排因其复杂性可归类为罕见的CCR,是罕见的CCR以平衡和/或不平衡形式在三代人中传递的例子。