Amelogenesis imperfecta: therapeutic strategy from primary to permanent dentition across case reports

BACKGROUND: Hereditary enamel defect diseases are regrouped under the name “Amelogenesis Imperfecta” (AIH). Both dentitions are affected. Clinical expression is heterogeneous and varies between patients. Mutations responsible for this multigene disease may alter various genes and the inheritance can...

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Detalles Bibliográficos
Autores principales: Toupenay, Steve, Fournier, Benjamin Philippe, Manière, Marie-Cécile, Ifi-Naulin, Chantal, Berdal, Ariane, de La Dure– Molla, Muriel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6003150/
https://www.ncbi.nlm.nih.gov/pubmed/29907114
http://dx.doi.org/10.1186/s12903-018-0554-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6003150/
https://www.ncbi.nlm.nih.gov/pubmed/29907114
http://dx.doi.org/10.1186/s12903-018-0554-y

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