Developmental milestones and cognitive trajectories in school-aged children with 16p11.2 deletion

Developmental milestones and cognitive trajectories in school-aged children with 16p11.2 deletion

Abstract Background 16p11.2 deletion syndrome (16p11.2DS) is a recurrent CNV that occurs de novo in approximately 70% of cases and confers risk for neurodevelopmental disorders, including intellectual disability (ID) and autism spectrum disorders (ASD). The current study focusses on developmental mi...

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Bibliographic Details
Main Authors: Jente Verbesselt, Jeroen Breckpot, Inge Zink, Ann Swillen
Format: Article
Language:English
Published: BMC 2025-06-01
Series:Journal of Neurodevelopmental Disorders
Subjects:
16p11.2 deletion syndrome
Copy number variants
Early development
Developmental trajectories
Deep phenotyping
Cognition
Online Access:https://doi.org/10.1186/s11689-025-09615-7
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https://doi.org/10.1186/s11689-025-09615-7

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