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A Case of Dentin Dysplasia with Full Mouth Rehabilitation: A 3-year Longitudinal Study
Dentin dysplasia, a rare hereditary disorder of dentin formation, is characterized by normal enamel but atypical dentin formation along with abnormal pulpal morphology. It is inherited as an autosomal dominant trait. It has been divided into two clinical entities: type I (radicular) and type II (cor...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Jaypee Brothers Medical Publishers
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4212168/ https://www.ncbi.nlm.nih.gov/pubmed/25356011 http://dx.doi.org/10.5005/jp-journals-10005-1248 |