Wilson's disease presenting with arthralgia: a case report
BackgroundsWilson's disease (WD) is a rare autosomal recessive disorder of copper metabolism characterized by impaired hepatic copper excretion and progressive multisystem copper accumulation. While hepatic and neuropsychiatric manifestations predominate, arthralgia as an initial presentation is unc...
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| Hauptverfasser: | , |
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| Format: | Artigo |
| Sprache: | Inglês |
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Frontiers Media S.A.
2026-04-01
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| Schriftenreihe: | Frontiers in Pediatrics |
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| Online-Zugang: | https://www.frontiersin.org/articles/10.3389/fped.2026.1781752/full |
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