Please use this identifier to cite or link to this item: http://repo.tma.uz/xmlui/handle/1/2507
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dc.contributor.authorHusayenova Husnobod., Abdujabborova Adashoy-
dc.date.accessioned2025-12-05T09:35:45Z-
dc.date.available2025-12-05T09:35:45Z-
dc.date.issued2025-
dc.identifier.issn2938-3765-
dc.identifier.urihttp://repo.tma.uz/xmlui/handle/1/2507-
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.en_US
dc.language.isoen_USen_US
dc.publisherWeb of Medicine: Journal of Medicine, Practice and Nursingen_US
dc.subjectDown syndrome, trisomy 21, prenatal diagnostics, rehabilitation, chromosomal anomalies, nootropic drugs.en_US
dc.titleCONGENITAL GENETIC DISORDER: MEDICAL AND SOCIAL ASPECTS OF DOWN SYNDROMEen_US
dc.typeArticleen_US
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