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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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| Publicado no: | Int J Clin Pediatr Dent |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Jaypee Brothers Medical Publishers
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5086016/ https://ncbi.nlm.nih.gov/pubmed/27843260 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5005/jp-journals-10005-1374 |
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