dc.contributor.author |
Zokirxodjayev Sherzod Yaxyayevich |
|
dc.date.accessioned |
2025-05-23T05:16:04Z |
|
dc.date.available |
2025-05-23T05:16:04Z |
|
dc.date.issued |
2025 |
|
dc.identifier.issn |
2181-7812 |
|
dc.identifier.uri |
http://repo.tma.uz/xmlui/handle/1/1504 |
|
dc.description.abstract |
Wilson’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.iso |
other |
en_US |
dc.publisher |
Toshkent tibbiyot akademiyasi axborotnomasi |
en_US |
dc.subject |
liver, copper metabolism, ceruloplasmin, liver failure, neurological symptoms. |
en_US |
dc.title |
"БОЛЕЗНЬ ВИЛЬСОНА – КОНОВАЛОВА: КЛИНИЧЕСКИЕ ПРОЯВЛЕНИЯ И МЕТОДЫ СОВРЕМЕННОЙ ДИАГНОСТИКИ" |
en_US |
dc.type |
Article |
en_US |