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dc.contributor.authorGulnoza Yusupova Amonillayevna, Shaxnoza Latipova Akbarbekovna-
dc.date.accessioned2020-02-29T10:04:11Z-
dc.date.available2020-02-29T10:04:11Z-
dc.date.issued2019-
dc.identifier.urihttp://repository.tma.uz/xmlui/handle/1/487-
dc.description.abstractApproximately 50 % of patients with primary ciliary dyskinesia have Kartagener syndrome, which classically described by a triad including dextrocardia, chronic sinusitis and bronchiectasis. Resynchronous dyskinesia, mucociliary clearance disturbances cause disturbances in the drainage function of the airways, which is the main cause of recurrent infections of the upper and lower respiratory tract-chronic rhinosinusitis, otitis media, chronic bronchitis with the formation of bronchiectasis, recurrent pneumonia. The given example of clinical observation showed the whole complexity of diagnosis of the Kartagener syndrome caused by the rarity of this disease.en_US
dc.language.isootheren_US
dc.publisherTashkenten_US
dc.relation.ispartofseriesУДК;-
dc.subjectKeywords: Kartagener syndrome; Genetic disease; Pneumonia; Ciliary dyskinesia; Dextracardiaen_US
dc.titleKartagener syndrome: an ususual condition with numerous difficult options: case report and rewiew of literatureen_US
dc.typeArticleen_US
Appears in Collections:Thesis, Articles

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