Global burden of Wilson disease: a comprehensive evidence synthesis
Abstract Background Wilson disease (WD) is a rare inherited copper metabolism disorder with variable prevalence worldwide. Many regions lack reliable data, leading to underestimation of burden. WD presents with hepatic, neurological, and psychiatric symptoms, but mental health impacts and economic c...
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| Hoofdauteurs: | , , , , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
BMC
2026-01-01
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| Reeks: | Orphanet Journal of Rare Diseases |
| Onderwerpen: | |
| Online toegang: | https://doi.org/10.1186/s13023-025-04185-2 |
| Tags: |
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