Rapidly Progressive Glomerulonephritis in Autosomal Dominant Polycystic Kidney Disease
Patients with autosomal dominant polycystic kidney disease (ADPKD) can suffer from the same causes of acute kidney injury as the general population. Affected individuals may present with hematuria and proteinuria (usually less than 1g/day). However, nephrotic syndrome and proliferative glomeruloneph...
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| Format: | Online |
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| Sprache: | Englisch |
| Veröffentlicht: |
Exon Publications
2024
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| Schlagworte: | |
| Online-Zugang: | https://directory.doabooks.org/handle/20.500.12854/138176 |
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