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Please use this identifier to cite or link to this item: http://repo.tma.uz/xmlui/handle/1/4334
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dc.contributor.authorAkhmedova, Dilorom-
dc.date.accessioned2026-06-12T07:51:34Z-
dc.date.available2026-06-12T07:51:34Z-
dc.date.issued2025-
dc.identifier.urihttp://repo.tma.uz/xmlui/handle/1/4334-
dc.description.abstractAlport syndrome is a rare but significant genetic disorder that affects multiple systems of the body, including the kidneys, hearing, and vision. It is one of the leading causes of inherited kidney failure, which progresses with age. Despite advancements in diagnostics and treatment, issues of early detection and appropriate therapy remain relevant in nephrology, ophthalmology, and otolaryngology. Effective treatment and early diagnosis are crucial for slowing disease progression and improving the quality of life of patients.en_US
dc.publisher11th Congress of the European Academy of Paediatric Societiesen_US
dc.titleALPORT SYNDROME: A MULTISYSTEM DISEASE AND THE POTENTIAL OF MODERN TREATMENT APPROACHESen_US
dc.typeThesisen_US
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