Gorlin-Goltz Syndrome

The Gorlin-Goltz syndrome (GGS) (the nevoid basal cell carcinoma syndrome) is a rare autosomal dominant syndrome caused due to mutations in the patched gene found on chromosome arm 9 q. It shows high penetrance and variable expressivity; is characterized by basal cell carcinomas, odontogenic keratoc...

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Detalles Bibliográficos
Autores principales: Mehta, DN, Raval, N, Patadiya, H, Tarsariya, V
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3991956/
https://www.ncbi.nlm.nih.gov/pubmed/24761254
http://dx.doi.org/10.4103/2141-9248.129064

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3991956/
https://www.ncbi.nlm.nih.gov/pubmed/24761254
http://dx.doi.org/10.4103/2141-9248.129064

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