Gorlin-Goltz syndrome: A rare case report

Gorlin-Goltz syndrome is an uncommon autosomal dominant inherited disorder characterized by numerous basal cell carcinomas, odontogenic keratocysts (OKCs) and musculoskeletal malformations. A rare case of this syndrome observed in a 13-year-old male patient is presented in which multiple OKCs were c...

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Detalles Bibliográficos
Autores principales: Pol, Chetan A, Ghige, Suvarna K, Kalaskar, Ritesh R, Gosavi, Suchitra R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3883343/
https://www.ncbi.nlm.nih.gov/pubmed/24403808
http://dx.doi.org/10.4103/0976-237X.123085

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3883343/
https://www.ncbi.nlm.nih.gov/pubmed/24403808
http://dx.doi.org/10.4103/0976-237X.123085

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