Dental approach for Apert syndrome in children: a systematic review

BACKGROUND: Apert Syndrome (AS), or type I acrocephalosyndactyly, is a rare, congenital craniosynostosis condition resulting from missense mutations in the gene encoding fibroblast growth factor receptor 2. It is characterized by three specific clinical features: brachycephalic skull; midface hypopl...

Descripción completa

Detalles Bibliográficos
Autores principales: López-Estudillo, Andrea-Stacy, Rosales-Bérber, Miguel-Ángel, Ruiz-Rodríguez, Socorro, Pozos-Guillén, Amaury, Noyola-Frías, Ángel, Garrocho-Rangel, Arturo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medicina Oral S.L. 2017
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5813983/
https://www.ncbi.nlm.nih.gov/pubmed/29053644
http://dx.doi.org/10.4317/medoral.21628

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5813983/
https://www.ncbi.nlm.nih.gov/pubmed/29053644
http://dx.doi.org/10.4317/medoral.21628

Ejemplares similares