Literature DB >> 32081578

An Overview of Craniosynostosis Craniofacial Syndromes for Combined Orthodontic and Surgical Management.

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.
Copyright © 2020 Elsevier Inc. All rights reserved.

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


  1 in total

1.  Midface advancement in an adult patient with Crouzon syndrome: Modified LeFort III + LeFort I osteotomy accompanied by genioplasty and nasal dorsum augmentation.

Authors:  Milad Etemadi Sh; Golnaz Tajmiri
Journal:  Dent Res J (Isfahan)       Date:  2022-04-27
  1 in total

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