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

Jente VerbesseltCynthia B SolotEllen Van Den HeuvelTerrence Blaine CrowleyVictoria GiuntaJeroen BreckpotDonna M McDonald-McGinnInge ZinkAnn Swillen
Published in: Genes (2023)
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.
Keyphrases
  • copy number
  • autism spectrum disorder
  • young adults
  • mental health
  • mitochondrial dna
  • randomized controlled trial
  • physical activity
  • gene expression
  • dna methylation
  • traumatic brain injury
  • congenital heart disease