Recurrent glomerulonephritis (GN) is an important cause of kidney allograft failure,
particularly in younger recipients. Approximately 15% of death-censored graft failures are …

The high frequency of monoclonal gammopathy in adult patients with C3 glomerulopathy
(C3G) emphasizes the role of monoclonal immunoglobulin (MIg) in the occurrence of renal …

Postinfectious glomerulonephritis is a common disorder that develops following an infection.
In the majority of cases, there is complete recovery of renal function within a few days to …

Membranoproliferative glomerulonephritis (MPGN) denotes a general pattern of glomerular
injury that is easily recognized by light microscopy. With additional studies, MPGN …

Atypical hemolytic uremic syndrome (aHUS), C3 glomerulopathy (C3G), and paroxysmal
nocturnal hemoglobinuria (PNH) are prototypical disorders of complement dysregulation …

Abstract C3 glomerulonephritis (C3GN) results from abnormalities in the alternative pathway
of complement, and it is characterized by deposition of C3 with absent or scant Ig deposition …

Objective To describe the clinicopathological features, complement abnormalities, triggers,
treatment, and outcomes of C3 glomerulopathy. Patients and Methods A total of 114 patients …

Background C3 glomerulonephritis (GN) is a proliferative GN resulting from glomerular
deposition of complement factors due to dysregulation of the alternative pathway of …

Monoclonal immunoglobulins (MIg) may play a causal role in C3 glomerulopathy (C3G) by
impairing regulation of the alternative pathway of complement. Ninety-five patients with C3G …

Until recently, membranoproliferative glomerulonephritis (MPGN) was clinically classified as
either primary, idiopathic MPGN or as secondary MPGN when an underlying aetiology was …