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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| Autores principales: | , , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Wolters Kluwer Medknow Publications
2018-01-01
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| Colección: | Contemporary Clinical Dentistry |
| Materias: | |
| Acceso en línea: | http://www.contempclindent.org/article.asp?issn=0976-237X;year=2018;volume=9;issue=3;spage=478;epage=483;aulast=Kumar |
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