A Comprehensive Craniofacial Study of 22q11.2 Deletion Syndrome

Volume: 96, Issue: 12, Pages: 1386 - 1391
Published: Jul 21, 2017
Abstract
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 3-dimensional (3D) facial surface scans, 2-dimensional (2D) clinical...
Paper Details
Title
A Comprehensive Craniofacial Study of 22q11.2 Deletion Syndrome
Published Date
Jul 21, 2017
Volume
96
Issue
12
Pages
1386 - 1391
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