| Literature DB >> 32081578 |
Shayna Azoulay-Avinoam1, Richard Bruun2, James MacLaine3, Veerasathpurush Allareddy4, Cory M Resnick5, Bonnie L Padwa6.
Abstract
This article provides an overview of epidemiology, genetics, and common orofacial features of those with craniosynostosis. Patients with craniosynostosis require several surgical procedures along with continuum of care. The earliest surgical interventions are done during the first few years of life to relieve the fused sutures. Midface advancement, limited phase of orthodontic treatment, and combined orthodontics/orthognathic surgery treatment are usually required during later years. This article presents several examples of cases with outcomes associated with these procedures.Entities:
Keywords: Apert syndrome; Craniofacial syndromes; Craniosynostosis; Crouzon syndrome; Maxillary distraction osteogenesis; Pfieffer syndrome
Year: 2020 PMID: 32081578 DOI: 10.1016/j.coms.2020.01.004
Source DB: PubMed Journal: Oral Maxillofac Surg Clin North Am ISSN: 1042-3699 Impact factor: 2.802