A Comprehensive Craniofacial Study of 22q11.2 Deletion Syndrome KU Leuven
© International & American Associations for Dental Research. The 22q11.2 deletion syndrome (22q11.2DS) is one of the most frequent microdeletion syndromes and presents with a highly variable phenotype. In most affected individuals, specific but subtle facial features can be seen. In this observational study, we aim to investigate the craniofacial and dental features of 20 children with a confirmed diagnosis of 22q11.2DS by analyzing ...