Gorlin-Goltz Syndrome

The Gorlin-Goltz syndrome (GGS) (the nevoid basal cell carcinoma syndrome—NBCCS) is a rare autosomal dominant syndrome caused due to mutations in the PTCH (patched) gene found on chromosome arm 9q. The syndrome, characterized by increased predisposition to develop basal cell carcinoma and associated...

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Detalles Bibliográficos
Autores principales: Pandeshwar, Padma, Jayanthi, K., Mahesh, D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3469076/
https://www.ncbi.nlm.nih.gov/pubmed/23082255
http://dx.doi.org/10.1155/2012/247239

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3469076/
https://www.ncbi.nlm.nih.gov/pubmed/23082255
http://dx.doi.org/10.1155/2012/247239

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