Results Central histology review determined 39 patients with C3 glomerulopathy, 31 with
immune-complex membranoproliferative GN, and ten with immune-complex GN. Patients …

Recent advances in our understanding of the disease pathology of membranoproliferative
glomerulonephritis has resulted in its re-classification as complement C3 glomerulopathy …

Introduction The reclassification of membranoproliferative glomerulonephritis (MPGN) into
immune-complex MPGN (IC-MPGN) and C3 glomerulopathy (C3G) has provided insights …

Background Complement component 3 glomerulopathy (C3G) is a disease with limited data
in children. We aimed to compare childhood C3G cases with adults. We also studied …

Abstract C3 glomerulopathy (C3G) is a clinicopathologic entity secondary to dysregulation of
the alternative complement pathway in plasma and the glomerular microenvironment. The …

Abstract Background C3 glomerulopathy (C3G) is a rare kidney disorder characterized by
predominant glomerular depositions of complement C3. C3G can be subdivided into dense …

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

Abstract Background C3 glomerulopathy (C3G) is characterized by predominant C3
deposits in glomeruli and dysregulation of the alternative pathway of complement. Half of …

Abstract Background C3 glomerulopathy (C3G) is characterized by heterogeneous clinical
presentation, outcome, and predominant C3 accumulation in glomeruli without significant …

Abstract C3 glomerulopathy (C3G) is a clinical spectrum that presents with a variety of
symptoms, ranging from a mild disease with asymptomatic microhematuria and/or …