Publication: Multiple odontogenic keratocysts associated with Gorlin-Goltz syndrome
creativeworkseries.issn | 1812-2027 | |
dc.contributor.author | Dixit, S | |
dc.contributor.author | Acharya, S | |
dc.contributor.author | Dixit, PB | |
dc.date.accessioned | 2025-08-07T06:42:33Z | |
dc.date.available | 2025-08-07T06:42:33Z | |
dc.date.issued | 2009 | |
dc.description | Dixit S1, Acharya S 2, Dixit PB3 1,3 Lecturer, Dental Department, Kathmandu Medical College, Sinamangal, Nepal, 2Lecturer, Dental Department, KIST Medical College, Lalitpur, Nepal. | |
dc.description.abstract | Abstract Gorlin-Goltz syndrome or Nevoid basal cell carcinoma syndrome is an autosomal dominant disorder with a predisposition to cancer. Features like basal cell carcinoma, odontogenic keratocysts, calcification of falx cerebri, bifid ribs, pits on palms and soles and hypertelorism are evident. A case of this rare disease seen on a 13 year old female patient is presented here, where multiple odontogenic keratocysts were causing disfigurement of the lower jaw as well as displacement and malocclusion of the lower teeth. Key words: Nevoid basal cell carcinoma syndrome, Gorlin-Goltz syndrome, Odentogenic keratocyst, Calcification of falx cerebri. | |
dc.identifier.uri | https://hdl.handle.net/20.500.14572/1355 | |
dc.language.iso | en_US | |
dc.publisher | Kathmandu University | |
dc.title | Multiple odontogenic keratocysts associated with Gorlin-Goltz syndrome | |
dc.type | Article | |
dspace.entity.type | Publication | |
local.article.type | Case Report | |
oaire.citation.endPage | 418 | |
oaire.citation.startPage | 414 | |
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relation.isJournalIssueOfPublication.latestForDiscovery | 0a79fcaf-b01a-4735-9a59-1858d4363bf5 | |
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