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Characterization of a de novo Supernumerary Neocentric Ring Chromosome Derived from Chromosome 7.
Louvrier, Camille; Egea, Grégory; Labalme, Audrey; Des Portes, Vincent; Gazzo, Sophie; Callet-Bauchu, Evelyne; Till, Marianne; Sanlaville, Damien; Edery, Patrick; Schluth-Bolard, Caroline.
Afiliação
  • Louvrier C; Laboratoire de Cytogx00E9;nx00E9;tique Constitutionnelle, Service de Gx00E9;nx00E9;tique, Centre de Biologie et de Pathologie Est, Bron, France.
Cytogenet Genome Res ; 147(2-3): 111-7, 2015.
Article em En | MEDLINE | ID: mdl-26669311
Supernumerary ring chromosomes (SRC) are usually derived from regions adjacent to the centromere. Their identification may be challenging, particularly in case of low mosaicism. Here, we report on a patient who was referred for major in utero growth retardation, severe developmental delay, facial dysmorphism, cleft palate, and hypospadias. The karyotype showed a small SRC in mosaic. The combination of FISH, M-FISH and array-CGH was necessary for a complete characterization of this SRC. M-FISH revealed that the SRC originated from chromosome 7. Array-CGH performed with a 400K oligonucleotide array showed a gain in region 7q22.1q31.1 present in low mosaic. This result was confirmed by FISH using BAC probes specific for chromosome 7. The SRC was a neocentric ring derived from 7q22.1q31.1 and was found in only 8% of the cells. This is the first patient carrying a mosaic neocentric SRC derived from the long arm of chromosome 7. Our study emphasizes the need to combine different techniques and to use adapted bioinformatic tools for low-mosaicism marker identification. It also contributes to the delineation of the partial trisomy 7q phenotype.
Assuntos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Cromossomos em Anel / Anormalidades Múltiplas / Cromossomos Humanos Par 7 / Mosaicismo Tipo de estudo: Observational_studies / Prognostic_studies Limite: Child / Child, preschool / Humans / Infant / Male / Newborn Idioma: En Revista: Cytogenet Genome Res Assunto da revista: GENETICA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Cromossomos em Anel / Anormalidades Múltiplas / Cromossomos Humanos Par 7 / Mosaicismo Tipo de estudo: Observational_studies / Prognostic_studies Limite: Child / Child, preschool / Humans / Infant / Male / Newborn Idioma: En Revista: Cytogenet Genome Res Assunto da revista: GENETICA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: França