Gorlin-Goltz Syndrome: A Case Report and Literature Review

Gorlin-Goltz syndrome (GGS) is an infrequent multisystemic disease with an autosomal dominant inherited disorder characterized by the presence of multiple keratocystic odontogenic tumors (KCOT) in the jaws, multiple basal cell nevi carcinomas, and skeletal abnormalities. Early diagnosis of Gorlin-Go...

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Detalles Bibliográficos
Autores principales: Al-Jarboua, Maha N, Al-Husayni, Abeer H, Al-Mgran, Mohammed, Al-Omar, Ahmad F
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2019
Materias:
Pediatric Surgery
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411325/
https://www.ncbi.nlm.nih.gov/pubmed/30891389
http://dx.doi.org/10.7759/cureus.3849

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411325/
https://www.ncbi.nlm.nih.gov/pubmed/30891389
http://dx.doi.org/10.7759/cureus.3849

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