Independent post-zygotic breaks of a dicentric chromosome result in mosaicism for an inverted duplication deletion 9p and terminal deletion 9p

被引:7
|
作者
Schlade-Bartusiak, Kamilla [1 ,2 ]
Tucker, Tracy [1 ]
Safavi, Holly [1 ]
Livingston, Janet [3 ]
van Allen, Margot I. [2 ,3 ]
Eydoux, Patrice [1 ]
Armstrong, Linlea [2 ,3 ]
机构
[1] Univ British Columbia, Dept Pathol & Lab Med, Vancouver, BC V5Z 4H4, Canada
[2] Child & Family Res Inst, Vancouver, BC, Canada
[3] Univ British Columbia, Dept Med Genet, Vancouver, BC V5Z 4H4, Canada
关键词
Inverted duplication deletion 9p; Mosaicism; Genotype-phenotype correlation; CLEAVAGE-STAGE EMBRYOS; INV DUP DEL(9P); CRITICAL REGION; CYTOGENETIC CHARACTERIZATION; MOLECULAR CHARACTERIZATION; TELOMERE CAPTURE; REARRANGEMENT; DELINEATION; PHENOTYPE; PATIENT;
D O I
10.1016/j.ejmg.2013.01.013
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Mosaicism with two cell lines having different rearrangements of the same chromosome is rare. Only a few cases of mosaicism have been described in association with chromosomal inverted duplication deletion (inv dup del) rearrangements. A well-established mechanism of formation of inv dup del rearrangements involves a dicentric intermediate, which undergoes breakage during cell division, generating cells with either an inv dup del or a simple deletion. A patient with developmental delay and dysmorphic features was found to carry two cell lines with rearrangements of 9p: an inv dup del 9p and a terminal deletion 9p. Microarray and FISH analysis showed that these cell lines do not constitute the reciprocal products of a single dicentric breakage event. We propose that independent post-zygotic breaks of a dicentric chromosome as a likely mechanism leading to the generation of the observed cell lines. The post-zygotic origin of the inv dup del rearrangements and the associated mosaicism can be a more frequent phenomenon than currently appreciated. Therefore, genotype-phenotype correlations in the inv dup del rearrangements need to take into account the possible presence of other abnormal cell lines during early development. (C) 2013 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:229 / 235
页数:7
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