Dentinogenesis imperfecta type I: A case report with literature review on nomenclature system

Dentinogenesis imperfecta (DI) is an inherited disorder affecting dentin. Defective dentin formation results in discolored teeth that are prone to attrition and fracture. Mutation in dentin sialophosphoprotein (DSPP) has been found to cause the dentin disorders DI - I and II (shields II and III). Ea...

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Detalles Bibliográficos
Autores principales: Devaraju, D, Devi, BK Yashoda, Vasudevan, Vijeev, Manjunath, V
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/PMC4211222/
https://www.ncbi.nlm.nih.gov/pubmed/25364163
http://dx.doi.org/10.4103/0973-029X.141363

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4211222/
https://www.ncbi.nlm.nih.gov/pubmed/25364163
http://dx.doi.org/10.4103/0973-029X.141363

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