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Kartagener syndrome: an ususual condition with numerous difficult options: case report and rewiew of literature

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dc.contributor.author Gulnoza Yusupova Amonillayevna, Shaxnoza Latipova Akbarbekovna
dc.date.accessioned 2020-02-29T10:04:11Z
dc.date.available 2020-02-29T10:04:11Z
dc.date.issued 2019
dc.identifier.uri http://repository.tma.uz/xmlui/handle/1/487
dc.description.abstract Approximately 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.iso other en_US
dc.publisher Tashkent en_US
dc.relation.ispartofseries УДК;
dc.subject Keywords: Kartagener syndrome; Genetic disease; Pneumonia; Ciliary dyskinesia; Dextracardia en_US
dc.title Kartagener syndrome: an ususual condition with numerous difficult options: case report and rewiew of literature en_US
dc.type Article en_US


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