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7p22.2 Microduplication: A Pathogenic CNV?
Partial duplication of the short arm of chromosome 7 is a rare chromosome rearrangement. The phenotype spectrum associated with this rearrangement is extremely variable even if in the last decade the use of high-resolution microarray technology for the investigation of patients carrying this rearran...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10297997/ https://www.ncbi.nlm.nih.gov/pubmed/37372471 http://dx.doi.org/10.3390/genes14061292 |
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author | Bauleo, Alessia Montesanto, Alberto Pace, Vincenza Guarasci, Francesco Apa, Rosalbina Brando, Rossella De Stefano, Laura Sestito, Simona Concolino, Daniela Falcone, Elena |
author_facet | Bauleo, Alessia Montesanto, Alberto Pace, Vincenza Guarasci, Francesco Apa, Rosalbina Brando, Rossella De Stefano, Laura Sestito, Simona Concolino, Daniela Falcone, Elena |
author_sort | Bauleo, Alessia |
collection | PubMed |
description | Partial duplication of the short arm of chromosome 7 is a rare chromosome rearrangement. The phenotype spectrum associated with this rearrangement is extremely variable even if in the last decade the use of high-resolution microarray technology for the investigation of patients carrying this rearrangement allowed for the identification of the 7p22.1 sub-band causative of this phenotype and to recognize the corresponding 7p22.1 microduplication syndrome. We report two unrelated patients that carry a microduplication involving the 7.22.2 sub-band. Unlike 7p22.1 microduplication carriers, both patients only show a neurodevelopmental disorder without malformations. We better characterized the clinical pictures of these two patients providing insight into the clinical phenotype associated with the microduplication of the 7p22.2 sub-band and support for a possible role of this sub-band in the 7p22 microduplication syndrome. |
format | Online Article Text |
id | pubmed-10297997 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-102979972023-06-28 7p22.2 Microduplication: A Pathogenic CNV? Bauleo, Alessia Montesanto, Alberto Pace, Vincenza Guarasci, Francesco Apa, Rosalbina Brando, Rossella De Stefano, Laura Sestito, Simona Concolino, Daniela Falcone, Elena Genes (Basel) Case Report Partial duplication of the short arm of chromosome 7 is a rare chromosome rearrangement. The phenotype spectrum associated with this rearrangement is extremely variable even if in the last decade the use of high-resolution microarray technology for the investigation of patients carrying this rearrangement allowed for the identification of the 7p22.1 sub-band causative of this phenotype and to recognize the corresponding 7p22.1 microduplication syndrome. We report two unrelated patients that carry a microduplication involving the 7.22.2 sub-band. Unlike 7p22.1 microduplication carriers, both patients only show a neurodevelopmental disorder without malformations. We better characterized the clinical pictures of these two patients providing insight into the clinical phenotype associated with the microduplication of the 7p22.2 sub-band and support for a possible role of this sub-band in the 7p22 microduplication syndrome. MDPI 2023-06-19 /pmc/articles/PMC10297997/ /pubmed/37372471 http://dx.doi.org/10.3390/genes14061292 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Case Report Bauleo, Alessia Montesanto, Alberto Pace, Vincenza Guarasci, Francesco Apa, Rosalbina Brando, Rossella De Stefano, Laura Sestito, Simona Concolino, Daniela Falcone, Elena 7p22.2 Microduplication: A Pathogenic CNV? |
title | 7p22.2 Microduplication: A Pathogenic CNV? |
title_full | 7p22.2 Microduplication: A Pathogenic CNV? |
title_fullStr | 7p22.2 Microduplication: A Pathogenic CNV? |
title_full_unstemmed | 7p22.2 Microduplication: A Pathogenic CNV? |
title_short | 7p22.2 Microduplication: A Pathogenic CNV? |
title_sort | 7p22.2 microduplication: a pathogenic cnv? |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10297997/ https://www.ncbi.nlm.nih.gov/pubmed/37372471 http://dx.doi.org/10.3390/genes14061292 |
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