Diagnostic and prognostic comparison of immune-complex-mediated membranoproliferative glomerulonephritis and C3 glomerulopathy

M Kovala, M Seppälä, A Räisänen-Sokolowski, S Meri… - Cells, 2023 - mdpi.com
… into dense deposit disease (DDD) and C3 glomerulonephritis (… can be observed in both
entities [11,15,33]. In PIGN, the … We chose to include both primary and secondary MPGN cases in …

Clusters not classifications: making sense of complement-mediated kidney injury

HT Cook, MC Pickering - Journal of the American Society of …, 2018 - journals.lww.com
entity, 3 showing isolated C3 without very dense deposits. The … in C3 glomerulopathy include
genetic and acquired factors. … In a study of over 300 patients with primary MPGN, the group …

[HTML][HTML] Nephritic factors: an overview of classification, diagnostic tools and clinical associations

F Corvillo, M Okrój, P Nozal, M Melgosa… - Frontiers in …, 2019 - frontiersin.org
… The stepwise formation of convertases from isolated complement … into Dense Deposit Disease
(DDD) and C3 glomerulonephritis (… A genetic and protein approach to study the Factor H-…

Recurrent postinfectious glomerulonephritis: an unusual evolution compatible with C3 glomerulopathy

JL Espinosa-Figueroa, M Cano-Megías… - Case …, 2018 - casereports.bmj.com
… , atypical haemolytic uraemic syndrome and a new entity called C3 … glomerular diseases in
which the primary pathogenic process is a … . Glomerulonephritis with isolated C3 deposits and …

C3 Glomerulopathies

C Licht, M Vivarelli, MR Khursigara, PD Walker - Pediatric Kidney Disease, 2023 - Springer
… , dense deposit disease and the more recently described C3 … the clinical picture of this new
disease entity, we suggest that in … to primary membranoproliferative glomerulonephritis of all …

Recurrent glomerulonephritis after renal transplantation: the clinical problem

B Infante, M Rossini, S Leo, D Troise, GS Netti… - International Journal of …, 2020 - mdpi.com
… of primary glomerulonephritis globally, and a common cause … dense deposits: type I, type
II or Dense Deposit Disease (… Risk factors for recurrence of C3 glomerulopathy after renal …

[HTML][HTML] C3 glomerulopathies: Dense deposit disease and C3 glomerulonephritis

T Kopel, DJ Salant - UpToDate. Weltham, MA, 2018 - medilib.ir
… of factor H or C3 genes increased the risk of developing the … nephritic syndrome (16 to 38
percent), isolated macroscopic … two disorders are thought to share a common pathogenesis [71]…

Coexistence of atypical hemolytic uremic syndrome with membranoproliferative glomerulonephritis and antineutrophil cytoplasmic antibodies-associated vasculitis

KP Sathe, KP Mehta - Saudi Journal of Kidney Diseases and …, 2016 - journals.lww.com
… of IgM, C3, and C1q deposits in the mesangium … disease spectrum. Uncontrolled activation
of the alternate complement pathway resulting from mutations of factor H gene or anti-factor H …

[HTML][HTML] Complement-mediated renal diseases after kidney transplantation-current diagnostic and therapeutic options in de novo and recurrent diseases

F Abbas, M El Kossi, JJ Kim, IS Shaheen… - World Journal of …, 2018 - ncbi.nlm.nih.gov
… The term aHUS is applied to a heterogenous group of diseases (Figure ​1) that share TMA
… in atypical hemolytic uremic syndrome, dense deposit disease, and C3 glomerulonephritis

Clinicopathological features of C3 glomerulopathy in children: a single-center experience

KA Drake, N Ellington, J Gattineni, JR Torrealba… - Pediatric …, 2020 - Springer
… —dense deposit disease (DDD) and C3 glomerulonephritis (… microscopy, distinction between
the two entities is made by EM [3]. … serologic and genetic testing for inherited and acquired …