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“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...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Hindawi
2020
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| Materias: | |
| 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 |