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Gorlin-Goltz Syndrome: A Rare Case Report
Gorlin-Goltz syndrome (GGS) is an autosomal dominant disorder with a high degree of penetrance and variable expressivity. It is a rare phakomatosis characterized by multiple odontogenic keratocysts (OKCs), bifid ribs, and other abnormalities. The incidence of the GGS is estimated at 1 in 57,000–1 in...
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| Publicado en: | Contemp Clin Dent |
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| Autores principales: | , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Medknow Publications & Media Pvt Ltd
2018
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6104368/ https://ncbi.nlm.nih.gov/pubmed/30166848 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/ccd.ccd_96_18 |
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