Gorlin-Goltz Syndrome: A Rare Case Report of a 11-Year-Old Child

Gorlin-Goltz Syndrome, also known as nevoid basal cell carcinoma syndrome (NBCCS), is an autosomal dominant trait caused due to mutations in the patched tumor suppressor gene (PTCH) gene found on the long arm of chromosome 9. The syndrome is characterized by the presence of odontogenic keratocysts (...

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Detalles Bibliográficos
Autores principales: Tandon, Sandeep, Chauhan, Yashwant, Sharma, Meenakshi, Jain, Manish
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Jaypee Brothers Medical Publishers 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5086016/
https://www.ncbi.nlm.nih.gov/pubmed/27843260
http://dx.doi.org/10.5005/jp-journals-10005-1374

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5086016/
https://www.ncbi.nlm.nih.gov/pubmed/27843260
http://dx.doi.org/10.5005/jp-journals-10005-1374

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