Profiles of atypical sensory processing in Angelman, Cornelia de Lange and Fragile X syndromes

Research output: Contribution to journalArticle

Authors

Colleges, School and Institutes

External organisations

  • Australian Rivers Institute, Griffith School of Environment, Griffith University

Abstract

BACKGROUND: There is growing evidence to suggest that children with neurodevelopmental disorders may evidence differences in their sensory processing. The aim of this study was to compare sensory processing patterns in three genetic syndromes associated with sensory difference.

METHODS: Sensory processing in Angelman syndrome (n = 91), Cornelia de Lange syndrome (n = 28) and Fragile X syndrome (n = 40) was examined using the informant report measure the Sensory Experiences Questionnaire (SEQ).

RESULTS: All three groups were associated with a heightened prevalence of unusual sensory processing in comparison with normative data, evidenced in over 80% of all participants. Cross-syndrome comparisons highlighted syndrome-specific sensory processing profiles, with heightened hypo responsivity in Cornelia de Lange syndrome and sensory seeking in Angelman syndrome.

CONCLUSIONS: The results have important implications for the understanding of sensory processing in genetic syndromes and the development of tailored behavioural interventions.

Bibliographic note

© 2019 MENCAP and International Association of the Scientific Study of Intellectual and Developmental Disabilities and John Wiley & Sons Ltd.

Details

Original languageEnglish
Pages (from-to)117-130
Number of pages14
JournalJournal of Intellectual Disability Research
Volume64
Issue number2
Early online date11 Dec 2019
Publication statusPublished - Feb 2020

Keywords

  • Angelman syndrome, Cornelia de Lange syndrome, Fragile X syndrome, Sensory processing