Adaptive living skills, sleep problems, and mental health disorders in adults with 22q11.21 deletion syndrome

Geraldine Leader, Andrea Curtin, Robert J. Shprintzen, Sally Whelan, Rory Coyne, Arlene Mannion

Research output: Contribution to a Journal (Peer & Non Peer)Articlepeer-review

7 Citations (Scopus)

Abstract

Background: 22q11.21 deletion syndrome (22q11DS) is a neurodevelopmental syndrome caused by a microdeletion of genes at the 22q11.21 locus. It has a prevalence of 1:2000. This study investigated the prevalence of adaptive living skills, sleep problems, and mental health disorders in adults with 22q11DS and examined the relationship between these factors. Methods: Parents with an adult son or daughter with 22q11DS completed the following: A bespoke Demographic Information Questionnaire, Sleep Questionnaire (SQ-SP), Psychopathology in Autism Checklist (PAC), and Activities of Daily Living (ADL) scale. Descriptive statistics, correlations, and one-way between groups analysis of variance (ANOVA) were conducted. Results: Mental health difficulties, sleep problems, and low levels of adaptive living skills are prevalent in adults with 22q11DS. Strong positive correlations were identified between sleep problems, depression, and anxiety subscale scores and moderate negative correlations between depression, psychosis, and activities of daily living skills. Conclusion: Adults with 22q11DS need screening and treatment for mental health and sleep problems.

Original languageEnglish
Article number104491
JournalResearch in Developmental Disabilities
Volume136
DOIs
Publication statusPublished - May 2023

Keywords

  • Conotruncal anomaly face syndrome
  • DiGeorge syndrome
  • Sedlačková syndrome
  • Velo-cardio-facial syndrome

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