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dc.contributor.authorAlkan A.
dc.contributor.authorMetin M.
dc.date.accessioned2020-06-21T09:15:14Z
dc.date.available2020-06-21T09:15:14Z
dc.date.issued2001
dc.identifier.issn1343-4934
dc.identifier.urihttps://doi.org/10.2334/josnusd.43.69
dc.identifier.urihttps://hdl.handle.net/20.500.12712/2669
dc.descriptionPubMed: 11383639en_US
dc.description.abstractTwo cases of double lip malformation, an uncommon oral anomaly, are presented, and the factors involved in the development, pathogenesis, diagnosis, and treatment of these uncommon lesions are reviewed. Double lip is usually associated with Ascher's syndrome, which is a rare disease with three more or less consistently associated abnormalities: double upper lip, blepharochalasis and enlargement of the thyroid. Two cases of double lip are reported; one of which was related with Ascher's syndrome, while the other had a traumatic origin.en_US
dc.language.isoengen_US
dc.relation.isversionof10.2334/josnusd.43.69en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleMaxillary double lip: report of two cases.en_US
dc.typereviewen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume43en_US
dc.identifier.issue1en_US
dc.identifier.startpage69en_US
dc.identifier.endpage72en_US
dc.relation.journalJournal of oral scienceen_US
dc.relation.publicationcategoryDiğeren_US


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