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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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| Vydáno v: | Int J Clin Pediatr Dent |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Jaypee Brothers Medical Publishers
2016
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| Témata: | |
| On-line přístup: | 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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