Craniofacial and oral alterations in patients with Neurofibromatosis 1

Neurofibromatosis type 1 (NF1) is one of the most common inherited syndromes. The literature on craniofacial alterations associated with NF1 has been limited and partially contradictory. This review is based on literature search and the results of the clinical study “Craniofacial and Oral Alteration...

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Detalles Bibliográficos
Autores principales: Visnapuu, Vivian, Peltonen, Sirkku, Alivuotila, Lotta, Happonen, Risto-Pekka, Peltonen, Juha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6085685/
https://www.ncbi.nlm.nih.gov/pubmed/30092804
http://dx.doi.org/10.1186/s13023-018-0881-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6085685/
https://www.ncbi.nlm.nih.gov/pubmed/30092804
http://dx.doi.org/10.1186/s13023-018-0881-8

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