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Molecular characterization of a rare analphoid supernumerary marker chromosome derived from 7q35 → qter: a case report
BACKGROUND: Analphoid supernumerary marker chromosomes (aSMC) constitute one of the smallest groups of SMC, and are characterized by a centromeric constriction but no detectable alpha-satellite DNA. These marker chromosomes cannot be properly identified by conventional banding techniques alone, and...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5123314/ https://www.ncbi.nlm.nih.gov/pubmed/27924152 http://dx.doi.org/10.1186/s13039-016-0295-z |
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author | Marques, Bárbara Ferreira, Cristina Brito, Filomena Pedro, Sónia Alves, Cristina Lourenço, Teresa Amorim, Marta Correia, Hildeberto |
author_facet | Marques, Bárbara Ferreira, Cristina Brito, Filomena Pedro, Sónia Alves, Cristina Lourenço, Teresa Amorim, Marta Correia, Hildeberto |
author_sort | Marques, Bárbara |
collection | PubMed |
description | BACKGROUND: Analphoid supernumerary marker chromosomes (aSMC) constitute one of the smallest groups of SMC, and are characterized by a centromeric constriction but no detectable alpha-satellite DNA. These marker chromosomes cannot be properly identified by conventional banding techniques alone, and molecular cytogenetic methods are necessary for a detailed characterization. Analphoid SMC derived from chromosome 7 are extremely rare, with only five cases reported so far. CASE PRESENTATION: In this work we report an aSMC involving the terminal long arm of chromosome 7 in a 10-year-old boy with multiple dysmorphic features and severe development delay. Cytogenetic analysis revealed a mosaic karyotype with the presence of an extra SMC, de novo, in 20% of lymphocytes and 73% of fibroblast cells. Next, we performed FISH analysis with multiple DNA probes and cCGH analysis. This identified the origin of the SMC as an analphoid marker resulting of invdup rearrangement of 7q35-qter region. Affimetrix CytoScan HD array analysis redefined the aSMC as a 15.42 Mb gain at 7q35-q36.3 (minimum tetraplicated region-chr7: 143,594,973-159,119,707; GRCh37/hg19) of maternal origin that encloses 67 OMIM genes, 16 of which associated to disease. Uniparental disomy of chromosome 7 (UPD 7) has been excluded. CONCLUSIONS: We report the first patient with an aSMC(7) derived from the terminal 7q region who has been molecularly and clinically full characterized. The use of SNParray in the characterization of SMC reveals to be a powerful tool, giving information not only about copy number variation but also about loss-of-heterozygosity and parental origin. We conclude that an integrated genome-wide copy number variation analysis, if possible associated to FISH and gene expression studies, could facilitate in the future the difficult task of establishing accurate genotype-phenotype correlations and help to improve genetic counselling. |
format | Online Article Text |
id | pubmed-5123314 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-51233142016-12-06 Molecular characterization of a rare analphoid supernumerary marker chromosome derived from 7q35 → qter: a case report Marques, Bárbara Ferreira, Cristina Brito, Filomena Pedro, Sónia Alves, Cristina Lourenço, Teresa Amorim, Marta Correia, Hildeberto Mol Cytogenet Case Report BACKGROUND: Analphoid supernumerary marker chromosomes (aSMC) constitute one of the smallest groups of SMC, and are characterized by a centromeric constriction but no detectable alpha-satellite DNA. These marker chromosomes cannot be properly identified by conventional banding techniques alone, and molecular cytogenetic methods are necessary for a detailed characterization. Analphoid SMC derived from chromosome 7 are extremely rare, with only five cases reported so far. CASE PRESENTATION: In this work we report an aSMC involving the terminal long arm of chromosome 7 in a 10-year-old boy with multiple dysmorphic features and severe development delay. Cytogenetic analysis revealed a mosaic karyotype with the presence of an extra SMC, de novo, in 20% of lymphocytes and 73% of fibroblast cells. Next, we performed FISH analysis with multiple DNA probes and cCGH analysis. This identified the origin of the SMC as an analphoid marker resulting of invdup rearrangement of 7q35-qter region. Affimetrix CytoScan HD array analysis redefined the aSMC as a 15.42 Mb gain at 7q35-q36.3 (minimum tetraplicated region-chr7: 143,594,973-159,119,707; GRCh37/hg19) of maternal origin that encloses 67 OMIM genes, 16 of which associated to disease. Uniparental disomy of chromosome 7 (UPD 7) has been excluded. CONCLUSIONS: We report the first patient with an aSMC(7) derived from the terminal 7q region who has been molecularly and clinically full characterized. The use of SNParray in the characterization of SMC reveals to be a powerful tool, giving information not only about copy number variation but also about loss-of-heterozygosity and parental origin. We conclude that an integrated genome-wide copy number variation analysis, if possible associated to FISH and gene expression studies, could facilitate in the future the difficult task of establishing accurate genotype-phenotype correlations and help to improve genetic counselling. BioMed Central 2016-11-25 /pmc/articles/PMC5123314/ /pubmed/27924152 http://dx.doi.org/10.1186/s13039-016-0295-z Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Marques, Bárbara Ferreira, Cristina Brito, Filomena Pedro, Sónia Alves, Cristina Lourenço, Teresa Amorim, Marta Correia, Hildeberto Molecular characterization of a rare analphoid supernumerary marker chromosome derived from 7q35 → qter: a case report |
title | Molecular characterization of a rare analphoid supernumerary marker chromosome derived from 7q35 → qter: a case report |
title_full | Molecular characterization of a rare analphoid supernumerary marker chromosome derived from 7q35 → qter: a case report |
title_fullStr | Molecular characterization of a rare analphoid supernumerary marker chromosome derived from 7q35 → qter: a case report |
title_full_unstemmed | Molecular characterization of a rare analphoid supernumerary marker chromosome derived from 7q35 → qter: a case report |
title_short | Molecular characterization of a rare analphoid supernumerary marker chromosome derived from 7q35 → qter: a case report |
title_sort | molecular characterization of a rare analphoid supernumerary marker chromosome derived from 7q35 → qter: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5123314/ https://www.ncbi.nlm.nih.gov/pubmed/27924152 http://dx.doi.org/10.1186/s13039-016-0295-z |
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