MUCOVISCIDOSIS A GENETIC DISEASE OF THE EXOCRINE GLANDS AND MANIFESTED AS A PATHOLOGY OF THE RESPIRATORY ORGANS

dc.contributor.authorBoynazarov Abbosjon Anvarovich
dc.contributor.authorKhabibova Nazira Nasullaevna
dc.date.accessioned2025-12-29T17:58:42Z
dc.date.issued2025-05-15
dc.description.abstractCystic fibrosis (CF), also called mucoviscidosis, is an autosomal recessive genetic disease that affects the exocrine function of the lungs, liver, pancreas, small bowel, sweat glands, and urogenital system. The condition causes thick mucus and other fluids to build up and clog different parts of the body, including the lungs and digestive tract. When mucus accumulates in the lungs of people with mucoviscidosis, it can cause frequent lung infections, which over time can cause severe damage to the lungs and inhibit breathing.
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dc.identifier.urihttps://webofjournals.com/index.php/5/article/view/4212
dc.identifier.urihttps://asianeducationindex.com/handle/123456789/24655
dc.language.isoeng
dc.publisherWeb of Journals Publishing
dc.relationhttps://webofjournals.com/index.php/5/article/view/4212/4169
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/4.0
dc.sourceWeb of Medicine: Journal of Medicine, Practice and Nursing ; Vol. 3 No. 5 (2025): WOM; 274-277
dc.source2938-3765
dc.subjectMucoviscidosis, viscous mucus, dry cough, pneumonia, chromosome 7, cystic fibrosis transmembrane regulator (CFTR) gene.
dc.titleMUCOVISCIDOSIS A GENETIC DISEASE OF THE EXOCRINE GLANDS AND MANIFESTED AS A PATHOLOGY OF THE RESPIRATORY ORGANS
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.typePeer-reviewed Article

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