Kartagener's Syndrome Presented with Nasal Obstruction: A Case Report

dc.contributor.authorAsilsoy, Suna
dc.contributor.authorKilicaslan, Buket
dc.contributor.authorOzer, Cem
dc.contributor.orcID0000-0002-6641-5300en_US
dc.contributor.researcherIDABH-1785-2020en_US
dc.contributor.researcherIDAAW-9958-2021en_US
dc.contributor.researcherIDAAM-7975-2020en_US
dc.date.accessioned2024-03-19T12:07:26Z
dc.date.available2024-03-19T12:07:26Z
dc.date.issued2014
dc.description.abstractThe nasal polyposis is a chronic inflammatory process of the nasal mucosa. Although it is rare in children, there may be also association with cystic fibrosis and primary ciliary dyskinesia. About 50% of primary ciliary dyskinesia patients develop situs inversus and it is known as Kartagener's syndrome. The Kartagener's sydrome is a rare autosomal recessive disorder characterized by sinusitis, bronchiectasis, situs inversus. Clinically, patients present to the otolaryngologist with nasal obstruction. We as pediatricians, should consider nasal polyposis as a rare cause of nasal obstruction in children. In the presence of recurrent upper and lower respiratory tract infections accompanying nasal polyposis, Kartagener's syndrome must be kept in mind as a rare reason.en_US
dc.identifier.eissn2602-3040en_US
dc.identifier.endpage945en_US
dc.identifier.issn2602-3032en_US
dc.identifier.issue4en_US
dc.identifier.startpage942en_US
dc.identifier.urihttp://hdl.handle.net/11727/11877
dc.identifier.volume39en_US
dc.identifier.wos000216471400041en_US
dc.language.isoturen_US
dc.relation.journalCUKUROVA MEDICAL JOURNALen_US
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergien_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectNasal polyposisen_US
dc.subjectkartagener's syndromeen_US
dc.subjectprimary ciliary dyskinesiaen_US
dc.subjectchildrenen_US
dc.titleKartagener's Syndrome Presented with Nasal Obstruction: A Case Reporten_US
dc.typearticleen_US

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