C3 glomerulonephritis
A histological subtype of C3 glomerulopathy characterized by C3 deposition in renal tissue in the absence or near-absence of immunoglobulin deposits in a patient with the classic clinical features of glomerulonephritis and the electron microscopic findings of predominant subendothelial occasionally subepithelial (so-called ”humps”) and intramembranous deposits but without the typical electron-dense deposits of dense deposit disease.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Reference: Access aggregated data from Orphanet at Orphadata.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version April 2024
Newly diagnosed with
C3 glomerulonephritis?
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