A cephalometric method to diagnosis the craniovertebral junction abnormalities in osteogenesis imperfecta patients

Osteogenesis imperfecta (OI) is a hereditary bone fragility disorder that in most patients is caused by mutations affecting collagen type I. Their typical oral and craneofacial characteristics (Dentinogenesis imperfecta type I and class III malocclusion), involve the dentist in the multidisciplinary...

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Detalles Bibliográficos
Autores principales: Ríos-Rodenas, Mercedes, de Nova, Joaquín, Gutiérrez-Díez, María-Pilar, Feijóo, Gonzalo, Mourelle, Maria-Rosa, Garcilazo, Mario, Ortega-Aranegui, Ricardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medicina Oral S.L. 2015
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4368004/
https://www.ncbi.nlm.nih.gov/pubmed/25810828
http://dx.doi.org/10.4317/jced.52126

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4368004/
https://www.ncbi.nlm.nih.gov/pubmed/25810828
http://dx.doi.org/10.4317/jced.52126

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