Please use this identifier to cite or link to this item: http://repo.tma.uz/xmlui/handle/1/1504
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dc.contributor.authorZokirxodjayev Sherzod Yaxyayevich-
dc.date.accessioned2025-05-23T05:16:04Z-
dc.date.available2025-05-23T05:16:04Z-
dc.date.issued2025-
dc.identifier.issn2181-7812-
dc.identifier.urihttp://repo.tma.uz/xmlui/handle/1/1504-
dc.description.abstractWilson’s disease is caused by an inherited defect in the liver’s ability to excrete copper into the bile. The resulting copper accumulation and copper toxicity lead to liver disease, and in some patients, brain damage. Patients are typically between the ages of 10 and 40 and suffer from liver disease, a neurological disorder such as motor disturbances or behavioral abnormalities, often in combination. Since Wilson’s disease (also known as Wilson-Konovalov disease) can be effectively treated, it is crucial for physicians to recognize and diagnose this condition.en_US
dc.language.isootheren_US
dc.publisherToshkent tibbiyot akademiyasi axborotnomasien_US
dc.subjectliver, copper metabolism, ceruloplasmin, liver failure, neurological symptoms.en_US
dc.title"БОЛЕЗНЬ ВИЛЬСОНА – КОНОВАЛОВА: КЛИНИЧЕСКИЕ ПРОЯВЛЕНИЯ И МЕТОДЫ СОВРЕМЕННОЙ ДИАГНОСТИКИ"en_US
dc.typeArticleen_US
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