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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...

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Autores principales: Bauleo, Alessia, Montesanto, Alberto, Pace, Vincenza, Guarasci, Francesco, Apa, Rosalbina, Brando, Rossella, De Stefano, Laura, Sestito, Simona, Concolino, Daniela, Falcone, Elena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
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.
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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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