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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...

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Detalles Bibliográficos
Autores principales: Khandelwal, Suneet, Gupta, Dheeraj, Likhyani, Lalit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Jaypee Brothers Medical Publishers 2014
Materias:
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

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