Crouzon syndrome Crouzon syndrome is an autosomal dominant genetic disorder. The first brachial arch is the affected arch. The brachial arches are also known as pharyngeal arches. This syndrome results from a mutation in chromosome 10. The name of this syndrome is derived from Octave Crouzon. He is the one who first described this condition....

Read moreTotal Calvarial Reconstruction (for Craniosynostosis) for 10 Month old baby with Crouzon Syndrome