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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
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 |
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author | Mascarell, Salomé Citterio, Hélène Martiano, Victor Friedlander, Lisa |
author_facet | Mascarell, Salomé Citterio, Hélène Martiano, Victor Friedlander, Lisa |
author_sort | Mascarell, Salomé |
collection | PubMed |
description | 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 form of AI. |
format | Online Article Text |
id | pubmed-8991759 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-89917592022-04-13 Full‐mouth rehabilitation choices depending on amelogenesis imperfecta's type: A familial case report Mascarell, Salomé Citterio, Hélène Martiano, Victor Friedlander, Lisa Clin Case Rep Case Reports 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 form of AI. John Wiley and Sons Inc. 2022-04-08 /pmc/articles/PMC8991759/ /pubmed/35425608 http://dx.doi.org/10.1002/ccr3.5459 Text en © 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Case Reports Mascarell, Salomé Citterio, Hélène Martiano, Victor Friedlander, Lisa Full‐mouth rehabilitation choices depending on amelogenesis imperfecta's type: A familial case report |
title | Full‐mouth rehabilitation choices depending on amelogenesis imperfecta's type: A familial case report |
title_full | Full‐mouth rehabilitation choices depending on amelogenesis imperfecta's type: A familial case report |
title_fullStr | Full‐mouth rehabilitation choices depending on amelogenesis imperfecta's type: A familial case report |
title_full_unstemmed | Full‐mouth rehabilitation choices depending on amelogenesis imperfecta's type: A familial case report |
title_short | Full‐mouth rehabilitation choices depending on amelogenesis imperfecta's type: A familial case report |
title_sort | full‐mouth rehabilitation choices depending on amelogenesis imperfecta's type: a familial case report |
topic | Case Reports |
url | 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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