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Language Profiles of School-Aged Children with 22q11.2 Copy Number Variants

Although it is known that copy number variants (CNVs) on chromosome 22, such as 22q11.2 deletion (22q11.2DS) and 22q11.2 duplication (22q11.2Dup) syndromes, are associated with higher risk for neurodevelopmental issues, few studies have examined the language skills across 22q11.2Dup nor compared the...

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Autores principales: Verbesselt, Jente, Solot, Cynthia B., Van Den Heuvel, Ellen, Crowley, T. Blaine, Giunta, Victoria, Breckpot, Jeroen, McDonald-McGinn, Donna M., Zink, Inge, Swillen, Ann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10048271/
https://www.ncbi.nlm.nih.gov/pubmed/36980951
http://dx.doi.org/10.3390/genes14030679
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author Verbesselt, Jente
Solot, Cynthia B.
Van Den Heuvel, Ellen
Crowley, T. Blaine
Giunta, Victoria
Breckpot, Jeroen
McDonald-McGinn, Donna M.
Zink, Inge
Swillen, Ann
author_facet Verbesselt, Jente
Solot, Cynthia B.
Van Den Heuvel, Ellen
Crowley, T. Blaine
Giunta, Victoria
Breckpot, Jeroen
McDonald-McGinn, Donna M.
Zink, Inge
Swillen, Ann
author_sort Verbesselt, Jente
collection PubMed
description Although it is known that copy number variants (CNVs) on chromosome 22, such as 22q11.2 deletion (22q11.2DS) and 22q11.2 duplication (22q11.2Dup) syndromes, are associated with higher risk for neurodevelopmental issues, few studies have examined the language skills across 22q11.2Dup nor compared them with the 22q11.2DS. The current study aims to characterize language abilities in school-aged children with 22q11.2Dup (n = 29), compared to age-matched children with 22q11.2DS (n = 29). Standardized language tests were administered, assessing receptive and expressive language skills across different language domains. Results indicate that children with 22q11.2Dup demonstrate significantly more language problems compared to the general population. Mean language skills were not significantly different among children with 22q11.2 CNVs in this cohort. While children with 22q11.2DS demonstrated language difficulties starting at the word level, the most common language problems in children with 22q11.2Dup started at the sentence level. Importantly, both expressive and receptive language as well as lexico-semantic and morphosyntactic domains were impaired in children with 22q11.2 CNVs. Early identification, therapeutic intervention, and follow-up of language impairments in children with 22q11.2Dup are recommended to support language development and to reduce longitudinal impact of language and communicative deficits.
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spelling pubmed-100482712023-03-29 Language Profiles of School-Aged Children with 22q11.2 Copy Number Variants Verbesselt, Jente Solot, Cynthia B. Van Den Heuvel, Ellen Crowley, T. Blaine Giunta, Victoria Breckpot, Jeroen McDonald-McGinn, Donna M. Zink, Inge Swillen, Ann Genes (Basel) Article Although it is known that copy number variants (CNVs) on chromosome 22, such as 22q11.2 deletion (22q11.2DS) and 22q11.2 duplication (22q11.2Dup) syndromes, are associated with higher risk for neurodevelopmental issues, few studies have examined the language skills across 22q11.2Dup nor compared them with the 22q11.2DS. The current study aims to characterize language abilities in school-aged children with 22q11.2Dup (n = 29), compared to age-matched children with 22q11.2DS (n = 29). Standardized language tests were administered, assessing receptive and expressive language skills across different language domains. Results indicate that children with 22q11.2Dup demonstrate significantly more language problems compared to the general population. Mean language skills were not significantly different among children with 22q11.2 CNVs in this cohort. While children with 22q11.2DS demonstrated language difficulties starting at the word level, the most common language problems in children with 22q11.2Dup started at the sentence level. Importantly, both expressive and receptive language as well as lexico-semantic and morphosyntactic domains were impaired in children with 22q11.2 CNVs. Early identification, therapeutic intervention, and follow-up of language impairments in children with 22q11.2Dup are recommended to support language development and to reduce longitudinal impact of language and communicative deficits. MDPI 2023-03-09 /pmc/articles/PMC10048271/ /pubmed/36980951 http://dx.doi.org/10.3390/genes14030679 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 Article
Verbesselt, Jente
Solot, Cynthia B.
Van Den Heuvel, Ellen
Crowley, T. Blaine
Giunta, Victoria
Breckpot, Jeroen
McDonald-McGinn, Donna M.
Zink, Inge
Swillen, Ann
Language Profiles of School-Aged Children with 22q11.2 Copy Number Variants
title Language Profiles of School-Aged Children with 22q11.2 Copy Number Variants
title_full Language Profiles of School-Aged Children with 22q11.2 Copy Number Variants
title_fullStr Language Profiles of School-Aged Children with 22q11.2 Copy Number Variants
title_full_unstemmed Language Profiles of School-Aged Children with 22q11.2 Copy Number Variants
title_short Language Profiles of School-Aged Children with 22q11.2 Copy Number Variants
title_sort language profiles of school-aged children with 22q11.2 copy number variants
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10048271/
https://www.ncbi.nlm.nih.gov/pubmed/36980951
http://dx.doi.org/10.3390/genes14030679
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