Literature DB >> 18088749

Craniofacial dysostosis syndromes: stages of reconstruction.

Jeffrey C Posnick1, Ramon L Ruiz, Paul S Tiwana.   

Abstract

The term "craniofacial dysostosis" is used in a general way to describe syndromal forms of craniosynostosis. These disorders are characterized by sutural involvement that not only includes the cranial vault but also extends into the skull base and midfacial skeletal structures. Craniofacial dysostosis syndromes have been described by Carpenter, Apert, Crouzon, Sathre-Chotzen, and Pfeiffer. Although the cranial vault and cranial base are believed to be the regions of primary involvement, there is also significant impact on midfacial growth and development. In addition to cranial vault dysmorphology, patients with these inherited conditions exhibit a characteristic "total midface" deficiency that is syndrome specific and must be addressed as part of the staged reconstructive approach.

Entities:  

Year:  2004        PMID: 18088749     DOI: 10.1016/j.coms.2004.08.004

Source DB:  PubMed          Journal:  Oral Maxillofac Surg Clin North Am        ISSN: 1042-3699            Impact factor:   2.802


  1 in total

1.  Long-term surgical cure of severe obstructive sleep apnea in an adult patient with craniofacial dysostosis (Crouzon's syndrome): a case report and literature review.

Authors:  Manolis Papagrigorakis; Georgios A Vilos; Charalabos Apostolidis; Euphemia Daskalopoulou; Manolis Vlachogiannis
Journal:  Sleep Breath       Date:  2010-08-26       Impact factor: 2.816

  1 in total

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