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dc.contributor.authorYildirim, Ugur
dc.contributor.authorAtmaca, Sinan
dc.contributor.authorKoyuncu, Mehmet
dc.date.accessioned2020-06-21T12:27:28Z
dc.date.available2020-06-21T12:27:28Z
dc.date.issued2019
dc.identifier.issn1049-2275
dc.identifier.issn1536-3732
dc.identifier.urihttps://doi.org/10.1097/SCS.0000000000005115
dc.identifier.urihttps://hdl.handle.net/20.500.12712/10929
dc.descriptionWOS: 000467717400025en_US
dc.descriptionPubMed: 30653037en_US
dc.description.abstractBranchial cleft anomalies occur due to insufficient closure of cavities during embryogenesis. These anomalies consist of cysts, sinuses, and fistulas, with the rarest type being fistulas. A 29-year-old male presented at the authors' clinic with a right-sided complete third branchial cleft fistula. Fistula track excision surgery was successfully performed and no recurrence was observed in the 12-month follow-up after the surgery. While second branchial cleft fistula is the most common, third and fourth brancial cleft fistulas are extremely rare. In addition, they are usually incomplete and almost always on the left side.en_US
dc.language.isoengen_US
dc.publisherLippincott Williams & Wilkinsen_US
dc.relation.isversionof10.1097/SCS.0000000000005115en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBranchial archesen_US
dc.subjectbranchial cleftsen_US
dc.subjectcongenital abnormalitiesen_US
dc.subjectnecken_US
dc.subjectpyriform sinusen_US
dc.titleRight-Sided Complete Third Branchial Cleft Fistulaen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume30en_US
dc.identifier.issue2en_US
dc.identifier.startpageE169en_US
dc.identifier.endpageE170en_US
dc.relation.journalJournal of Craniofacial Surgeryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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