CONGENITAL GENETIC DISORDER: MEDICAL AND SOCIAL ASPECTS OF DOWN SYNDROME

dc.contributor.authorHusayenova Husnobod
dc.contributor.authorAbdujabborova Adashoy
dc.date.accessioned2025-12-29T17:58:39Z
dc.date.issued2025-05-13
dc.description.abstractDown syndrome (trisomy 21) is a genetic disorder caused by an extra chromosome in the 21st pair of chromosomes. This syndrome leads to delays in intellectual and physical development, distinctive facial features, and other health issues. Prenatal tests are available for early detection of the condition, and early interventions can improve the development of patients. The article provides information about the diagnosis, development, and treatment methods of Down syndrome.
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dc.identifier.urihttps://webofjournals.com/index.php/5/article/view/4177
dc.identifier.urihttps://asianeducationindex.com/handle/123456789/24645
dc.language.isoeng
dc.publisherWeb of Journals Publishing
dc.relationhttps://webofjournals.com/index.php/5/article/view/4177/4133
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; 227-231
dc.source2938-3765
dc.subjectDown syndrome, trisomy 21, prenatal diagnostics, rehabilitation, chromosomal anomalies, nootropic drugs.
dc.titleCONGENITAL GENETIC DISORDER: MEDICAL AND SOCIAL ASPECTS OF DOWN SYNDROME
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.typePeer-reviewed Article

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