Brittle teeth with brittle bone in a family for four generations: Case report and literature review

Dentinogenesis imperfect (DI) is a hereditary dentine disorder affecting both deciduous and permanent teeth. DI is caused by mutations in genes encoding for type I collagen leading to discoloration of teeth. Shield around 30 years ago classified DI into 3 types (type I, II, and III). DI type I is as...

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Detalles Bibliográficos
Autores principales: Shilpa, P. S., David, Chaya M., Kaul, Rachna, Sanjay, C. J., Narayan, B. K. Ram
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3425106/
https://www.ncbi.nlm.nih.gov/pubmed/22919223
http://dx.doi.org/10.4103/0976-237X.96822

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3425106/
https://www.ncbi.nlm.nih.gov/pubmed/22919223
http://dx.doi.org/10.4103/0976-237X.96822

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