Full‐mouth rehabilitation choices depending on amelogenesis imperfecta's type: A familial case report

Amelogenesis imperfecta, a rare disease, represents inherited, congenital defects that primarily affect enamel with esthetic and functional impairment affecting everyday life. We present oral rehabilitation of a mother and her son, respectively, suffering from an hypoplastic and an hypocalcified for...

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Detalles Bibliográficos
Autores principales: Mascarell, Salomé, Citterio, Hélène, Martiano, Victor, Friedlander, Lisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8991759/
https://www.ncbi.nlm.nih.gov/pubmed/35425608
http://dx.doi.org/10.1002/ccr3.5459

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8991759/
https://www.ncbi.nlm.nih.gov/pubmed/35425608
http://dx.doi.org/10.1002/ccr3.5459

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