Patient-reported outcome measures in individuals with amelogenesis imperfecta: a systematic review

PURPOSE: Amelogenesis imperfecta (AI) is a hereditary condition which affects the composition and structure of enamel in terms of hypoplasia and/or hypomineralization. The condition severely affects patients facing such difficulties as hypersensibility, loss of tooth substance and poor aesthetics. T...

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Detalles Bibliográficos
Autores principales: Appelstrand, S. B., Robertson, A., Sabel, N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Systematic Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9750902/
https://www.ncbi.nlm.nih.gov/pubmed/35896941
http://dx.doi.org/10.1007/s40368-022-00737-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9750902/
https://www.ncbi.nlm.nih.gov/pubmed/35896941
http://dx.doi.org/10.1007/s40368-022-00737-3

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