Apert syndrome: a case report in pediatric dentistry
DOI:
https://doi.org/10.15381/os.v14i2.2934Keywords:
Apert syndrome, craniosynostosis, Fibroblast growth factor receptor 2 gene.Abstract
Apert syndrome accounts for 5% of all craniosynostosis syndromes and shows a prevalence of 1 in 60000 live births. Is one of the five craniosynostosis syndromes associated with single mutations in the Fibroblast Growth Factor Receptor 2 (FGF-R2) gene, with chromosomal localization at 10q26. The purpose of this paper was to describe a case of Apert syndrome, show Pediatric dentistry managementand discuss their craniofacial features in an 8-year-old boy who presented Craniosynostosis, turribrachycephaly, syndactylies of the hands and feet, with multiple intraoral features.Downloads
Downloads
Published
Issue
Section
License
Copyright (c) 2011 Rocío Contreras Linares, Fredy Mas Gáslac, Daniela Jota Altamirano
This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.
AUTHORS RETAIN THEIR RIGHTS:
a. Authors retain their trade mark rights and patent, and also on any process or procedure described in the article.
b. Authors retain their right to share, copy, distribute, perform and publicly communicate their article (eg, to place their article in an institutional repository or publish it in a book), with an acknowledgment of its initial publication in the Odontología Sanmarquina.
c. Authors retain theirs right to make a subsequent publication of their work, to use the article or any part thereof (eg a compilation of his papers, lecture notes, thesis, or a book), always indicating the source of publication (the originator of the work, journal, volume, number and date).