Mutiple keratocystic odontogenic tumors (KCOT) in a patient with Gorlin syndrome: a case report with late presentation and absence of skin manifestations

BACKGROUND: Gorlin syndrome is a rare autosomal dominant syndrome characterized by multiple basal cell carcinomas, keratocystic odontogenic tumors (KOT) and falx cerebral calcifications, which occur due to mutation in PTCH gene. CASE PRESENTATION: A 36 year old Asian patient presented with jaw swell...

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Detalles Bibliográficos
Autores principales: Hashmi, Atif Ali, Edhi, Muhammad Muzzammil, Faridi, Naveen, Hosein, Mervyn, Khan, Mehmood
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4957855/
https://www.ncbi.nlm.nih.gov/pubmed/27448602
http://dx.doi.org/10.1186/s13104-016-2166-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4957855/
https://www.ncbi.nlm.nih.gov/pubmed/27448602
http://dx.doi.org/10.1186/s13104-016-2166-4

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