Odontogenic Keratocysts in Gorlin–Goltz Syndrome: A Case Report

Gorlin–Goltz syndrome is an autosomal dominant inherited condition comprising the principle triad of basal cell carcinomas, multiple jaw keratocysts, and skeletal anomalies. The presence of jaw cysts are the early diagnostic feature of this syndrome, and this can be incidentally identified by routin...

Descripción completa

Detalles Bibliográficos
Autores principales: Chandran, Satheesh, Marudhamuthu, Karthikeyan, Riaz, R, Balasubramaniam, Saravanan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dentmedpub Research and Printing Co 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4516062/
https://www.ncbi.nlm.nih.gov/pubmed/26225111

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4516062/
https://www.ncbi.nlm.nih.gov/pubmed/26225111

Ejemplares similares