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Famlial nonsyndromic oligodontia

Oligodontia is one of the most common developmental abnormalities in humans. The present case report highlights the features of oligodontia in a 12-year-old male patient which was managed successfully with multidisciplinary approach. Familial oligodontia represents as an absence of varying numbers o...

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Detalles Bibliográficos
Autores principales: Punithavathy, John, John B., Priya, Geetha, Elango, Indhumathi, Stalin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3514934/
https://www.ncbi.nlm.nih.gov/pubmed/23230360
http://dx.doi.org/10.4103/0976-237X.101088

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