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dc.contributor.authorTolibjonova Malika Xusanovna-
dc.date.accessioned2026-04-06T17:39:55Z-
dc.date.available2026-04-06T17:39:55Z-
dc.date.issued2025-
dc.identifier.issn2181-7812-
dc.identifier.urihttp://repo.tma.uz/xmlui/handle/1/3212-
dc.description.abstractCystic fibrosis is a hereditary disease that affects the exocrine glands, leading to the production of thick and sticky mucus in the respiratory system, digestive tract, and other organs. In children, the disease manifests from an early age and requires timely diagnosis and treatment. Without adequate therapy, cystic fibrosis can lead to severe complications, disability, and a significant decrease in quality of life. This article discusses the epidemiology, causes, diagnosis, symptoms, and modern treatment methods of this disease.en_US
dc.publisherToshkent tibbiyot akademiyasi axborotnomasien_US
dc.subjectcystic fibrosis, children, genetic disease, disability, diagnosis, treatmenten_US
dc.titleCYSTIC FIBROSIS IN CHILDREN: ASEVERE DISEASE LEADING TO DISABILITYen_US
dc.typeArticleen_US
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