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Achondroplasia with multiple supplemental supernumerary teeth and multiple talon cusps: A rare case report

Achondroplasia is the most common cause of dwarfism, which is inherited as an autosomal dominant disorder, caused by genetic mutation in fibroblast growth factor 3, leading to defective maturation of chondrocytes. It is known to be associated with various oral and dental manifestations such as delay...

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Detalles Bibliográficos
Autores principales: Raviraj, Jayam, Suman, Venkata, Suresh, Dirasantchu, Kartik, K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5504876/
https://www.ncbi.nlm.nih.gov/pubmed/28702065