“Isolated” Amelogenesis Imperfecta Associated with DLX3 Mutation: A Clinical Case

Amelogenesis imperfecta (AI) represents rare tooth anomalies that affect the quality and/or quantity of the enamel. Clinical phenotypes display a wide spectrum, ranging from mild color changes to severe structural alterations with daily pain. However, all affect the quality of life because of mechan...

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Detalles Bibliográficos
Autores principales: Bonnet, Anne-Laure, Sceosole, Kevin, Vanderzwalm, Arabelle, Silve, Caroline, Collignon, Anne-Margaux, Gaucher, Celine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7424401/
https://www.ncbi.nlm.nih.gov/pubmed/32832172
http://dx.doi.org/10.1155/2020/8217919

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7424401/
https://www.ncbi.nlm.nih.gov/pubmed/32832172
http://dx.doi.org/10.1155/2020/8217919

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