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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Médium:	Online
Jazyk:	angličtina
Vydáno:	Exon Publications 2024
Témata:	Rapidly Progressive Glomerulonephritis Autosomal Dominant Polycystic Kidney Disease acute kidney injury MJR
On-line přístup:	https://directory.doabooks.org/handle/20.500.12854/138176
Tagy:	Přidat tag Žádné tagy, Buďte první, kdo vytvoří štítek k tomuto záznamu!