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Eur J Med Genet ; 56(5): 229-35, 2013 May.
Artigo em Inglês | MEDLINE | ID: mdl-23416622

RESUMO

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.


Assuntos
Transtornos Cromossômicos/genética , Mosaicismo , Deleção Cromossômica , Inversão Cromossômica , Mapeamento Cromossômico , Cromossomos Humanos Par 9/genética , Feminino , Duplicação Gênica , Rearranjo Gênico , Estudos de Associação Genética , Humanos , Hibridização in Situ Fluorescente , Recém-Nascido , Análise em Microsséries
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