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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Bibliographic Details
Format: Online
Language:English
Published: Exon Publications 2024
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Online Access:https://directory.doabooks.org/handle/20.500.12854/138176
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