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dc.contributor.authorCelenk, P
dc.contributor.authorAlkan, A
dc.contributor.authorCanger, EM
dc.contributor.authorGunhan, O
dc.date.accessioned2020-06-21T15:37:21Z
dc.date.available2020-06-21T15:37:21Z
dc.date.issued2005
dc.identifier.issn1079-2104
dc.identifier.urihttps://doi.org/10.1016/j.tripleo.2004.07.003
dc.identifier.urihttps://hdl.handle.net/20.500.12712/21208
dc.descriptionWOS: 000226451900015en_US
dc.descriptionPubMed: 15660093en_US
dc.description.abstractTuberous sclerosis is a rare congenital disorder with an incidence of 1 in 6000 births. The classic triad is seizure, mental deficiency, and angiofibromas. Orofacial manifestations include fibrous hyperplasia, hemangioma, bifid uvula, cleft lip and palate, macroglossia, high arched palate, and enamel defects. Benign tumors of the jaws including desmoplastic fibroma, calcifying odontogenic tumor, and odontogenic myxoma have been recently reported in tuberous sclerosis. This case report adds fibrolipomatous hamartoma of the mandible to this list.en_US
dc.language.isoengen_US
dc.publisherMosby, Incen_US
dc.relation.isversionof10.1016/j.tripleo.2004.07.003en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleFibrolipomatous hamartoma in a patient with tuberous sclerosis: Report of a caseen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume99en_US
dc.identifier.issue2en_US
dc.identifier.startpage202en_US
dc.identifier.endpage206en_US
dc.relation.journalOral Surgery Oral Medicine Oral Pathology Oral Radiology and Endodonticsen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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