A RARE MULTILOCULAR CYSTIC DISEASE OF MANDIBLE: CHERUBISM

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dc.authoridGumus, Nazim/0000-0002-2422-6456
dc.contributor.authorGumus, Nazim
dc.contributor.authorYilmaz, Sarper
dc.date.accessioned2024-10-26T18:05:17Z
dc.date.available2024-10-26T18:05:17Z
dc.date.issued2014
dc.departmentSivas Cumhuriyet Üniversitesi
dc.description.abstractCherubism is a rare skeletal dysplasia located to the maxilla and mandible which is characterized by bilateral, symmetric, fibro-osseous and multilocular cystic lesions. In most of the cases, dominant mutations are detected in the SH3BP2 gene on chromosome 4p. While affected children seem to be clinically normal at birth, whose jaws start swelling and enlargement between 2 and 7 years of age. Full round cheek and upward tilting of the eyes consist of typical appearance of children. Apart from various cystic lesions of mandible, cherubism is a tumor which regresses spontaneously, ossifies over time and has a likelihood for leaving unrecognizable remnants after years, although radiologically, extensive bone involvement appears. Presented here was a patient who suffered from this rare disease and his clinical findings.
dc.identifier.endpage126
dc.identifier.issn2528-8644
dc.identifier.issue3
dc.identifier.startpage124
dc.identifier.urihttps://hdl.handle.net/20.500.12418/28911
dc.identifier.volume22
dc.identifier.wosWOS:000416771300008
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.language.isotr
dc.publisherMedknow Publications & Media Pvt Ltd
dc.relation.ispartofTurkish Journal of Plastic Surgery
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectcherubism
dc.subjectmandible
dc.subjectmultilocular bone cyst
dc.titleA RARE MULTILOCULAR CYSTIC DISEASE OF MANDIBLE: CHERUBISM
dc.typeArticle

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