ORAL FINDINGS IN PATIENTS WITH APERT SYNDROME

INTRODUCTION: The Apert syndrome is a rare disorder of autosomal dominant inheritance caused by mutations in the FGFR2 gene at locus 10q26; patients with this syndrome present severe syndactyly, exophthalmia, ocular hypertelorism and hypoplastic midface with Class III malocclusion, besides systemic...

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Detalles Bibliográficos
Autores principales: Dalben, Gisele da Silva, Neves, Lucimara Teixeira das, Gomide, Marcia Ribeiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Faculdade de Odontologia de Bauru da Universidade de São Paulo 2006
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4327301/
https://www.ncbi.nlm.nih.gov/pubmed/19089249
http://dx.doi.org/10.1590/S1678-77572006000600014

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4327301/
https://www.ncbi.nlm.nih.gov/pubmed/19089249
http://dx.doi.org/10.1590/S1678-77572006000600014

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