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Billet publié sur Twitter/X le 21/04/2022 05:37

Twitter/X Publication avec DOI crossref Extrait cité dans le billet Lien intégré au billet Termes sur l’autisme

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Johan Lundin Kleberg, Deborah Riby, Christine Fawcett, Hanna Björlin Avdic, Matilda A. Frick, Karin C. Brocki, Jens Högström, Eva Serlachius, et al. (2023). Williams syndrome: reduced orienting to other’s eyes in a hypersocial phenotype. Journal of Autism and Developmental Disorders, 53(7), 2786-2797. Springer Science and Business Media LLC.

Date de publication
20/04/2022
Identifiant
10.1007/s10803-022-05563-6
Auteurs
Johan Lundin Kleberg, Deborah Riby, Christine Fawcett, Hanna Björlin Avdic, Matilda A. Frick, Karin C. Brocki, Jens Högström, Eva Serlachius, Ann Nordgren, Charlotte Willfors
Source
Journal of Autism and Developmental Disorders
Détails
53(7), 2786-2797
Type de référence
article
Éditeur
Springer Science and Business Media LLC
Source de métadonnées
crossref

Résumé

Abstract Williams syndrome (WS) is a rare genetic condition associated with high sociability, intellectual disability, and social cognitive challenges. Attention to others’ eyes is crucial for social understanding. Orienting to, and from other’s eyes was studied in WS (n = 37, mean age = 23, age range 9–53). The WS group was compared to a typically developing comparison participants (n = 167) in stratified age groups from infancy to adulthood. Typically developing children and adults were quicker and more likely to orient to eyes than the mouth. This bias was absent in WS. The WS group had reduced peak saccadic velocities, indicating hypo-arousal. The current study indicates reduced orienting to others’ eyes in WS, which may affect social interaction skills.

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