The Wilson's disease - etiology, symptoms in various organs, diagnosis, treatment, prognosis
Introduction: Wilson disease (WD) is a genetic disorder of copper metabolism caused by ATP7B gene mutations, impairing copper excretion and leading to copper accumulation in organs. It affects children and adults, causing liver damage, cirrhosis, neuropsychiatric symptoms, and, if untreated, deat...
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| Autors principals: | , , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Kazimierz Wielki University
2025-01-01
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| Col·lecció: | Journal of Education, Health and Sport |
| Matèries: | |
| Accés en línia: | https://apcz.umk.pl/JEHS/article/view/56733 |
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