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...

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Detaylı Bibliyografya
Yayımlandı:Med Oral Patol Oral Cir Bucal
Asıl Yazarlar: López-Estudillo, Andrea-Stacy, Rosales-Bérber, Miguel-Ángel, Ruiz-Rodríguez, Socorro, Pozos-Guillén, Amaury, Noyola-Frías, Ángel, Garrocho-Rangel, Arturo
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Medicina Oral S.L. 2017
Konular:
Review
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5813983/
https://ncbi.nlm.nih.gov/pubmed/29053644
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4317/medoral.21628
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