Implant-based oral rehabilitation of a variant model of type I dentinal dysplasia: A rare case report

Dentin dysplasia is an exceptionally rare, autosomal-dominant, hereditary condition, primarily characterized by defective dentin formation affecting both the deciduous and permanent dentitions. The etiology remains imprecise to date, in spite of the numerous hypotheses put forward and the constant u...

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Detalles Bibliográficos
Autores principales: Nettem, Sowmya, Nettemu, Sunil Kumar, Basha, K., Venkatachalapathi, S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4163832/
https://www.ncbi.nlm.nih.gov/pubmed/25225567

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