This study presents the results of an examination of patients with Wilson-Konovalov disease, a rare autosomal recessive disorder characterized by copper accumulation in the liver, brain, and other organs. Biochemical parameters and instrumental diagnostic methods were evaluated in accordance with international guidelines, which require further confirmation of the diagnosis through molecular genetic testing. Specific ultrasound markers of liver damage were identified, which determine the clinical presentation of this disease in children.
| Mualliflar | MURATKHOZHAYEVA Akida Valievna, KHAMDAMOVA Yokuthon Sirozhiddin qizi |
|---|---|
| Jurnal | Journal of Biomedicine and Practice – Biomeditsina va amaliyot jurnali |
| Nashr sanasi | 2025-08-09 |
| Jild | 10 |
| Son | 3/1 |
| Til | Rus |
болезнь Вильсона-Коновалова, диагностика, клиническое течение, дети, поражение гепатобилиарной системы., Wilson-Konovalov disease, diagnosis, clinical course, children, hepatobiliary system involvement. МУРАТХОЖАЕВА Акида Валиевна, Vilson-Konovalov kasalligi, diagnostika, klinik kechish, bolalar, gepatobiliar tizim shikastlanishi.
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