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Gorlin Syndrome with Bilateral Polydactyly: A Rare Case Report
Gorlin's syndrome is a rare disorder transmitted as an autosomal dominant trait. It is characterized by multiple disorders involving multiple systems. We present a case of 11-year-old male child presenting with multiple odontogenic keratocyst to the dental clinic. Retrograde diagnosis of Gorlin...
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| Hauptverfasser: | , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Jaypee Brothers Medical Publishers
2013
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4086603/ https://ncbi.nlm.nih.gov/pubmed/25206225 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5005/jp-journals-10005-1221 |
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