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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...
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| Publicado no: | J Int Oral Health |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Dentmedpub Research and Printing Co
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4516062/ https://ncbi.nlm.nih.gov/pubmed/26225111 |
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