Toward autism spectrum disorders and Williams-Beuren syndrome co-occurrence condition in Tunisian patients: Genetic insights

Toward autism spectrum disorders and Williams-Beuren syndrome co-occurrence condition in Tunisian patients: Genetic insights

IntroductionWilliams-Beuren syndrome (WBS) is a rare genetic disorder characterized by congenital heart defects, dysmorphic features, intellectual delay, and a distinctive social behavioral profile. This highly recurrent and homogeneous phenotype has been curiously reported to be associated with aut...

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Main Authors: Rim Khelifi, Afef Jelloul, Houda Ajmi, Wafa Slimani, Sarra Dimassi, Khouloud Rjiba, Manel Dardour, Moez Gribaa, Ali Saad, Soumaya Mougou-Zerelli
Format: Article
Language:English
Published: AIMS Press 2024-11-01
Series:AIMS Molecular Science
Subjects:
cgh-array
williams beuren-syndrome
autistic traits
hip1
Online Access:https://www.aimspress.com/article/doi/10.3934/molsci.2024023
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https://www.aimspress.com/article/doi/10.3934/molsci.2024023

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