Cephalometric analysis of hard and soft tissues in a 12-year-old syndromic child: A case report and update on dentofacial features of Crouzon syndrome

• Hoofdauteurs: K Nagaraju (Auteur), E Ranadheer (Auteur), P Suresh (Auteur), S P Tarun (Auteur)
• Formaat: Boek
• Gepubliceerd in: Wolters Kluwer Medknow Publications, 2011-01-01T00:00:00Z.
• Onderwerpen: article
• Online toegang: Connect to this object online.

Crouzon syndrome or craniofacial dysostosis is a rare syndrome characterized by craniosynostosis, midfacial hypoplasia and exophthalmia. The abnormalities found in this syndrome change too much from case to case depending on the suture fusion order. We report a case of a 12 year old child and a moth...