Alport syndrome complicated with IgA nephropathy: a case report
Alport syndrome (AS) and immunoglobulin A (IgA) nephropathy (IgAN) are distinct renal disorders characterized by hematuria and proteinuria. AS is a rare hereditary condition caused by mutations in genes encoding collagen IV α-chains, leading to abnormalities of the glomerular basement membrane. Howe...
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| Hoofdauteurs: | , |
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| Formaat: | Artigo |
| Taal: | Inglês |
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Frontiers Media S.A.
2026-02-01
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| Reeks: | Frontiers in Medicine |
| Onderwerpen: | |
| Online toegang: | https://www.frontiersin.org/articles/10.3389/fmed.2026.1739845/full |
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