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Overview of C3 Glomerulopathy

Overview
Journal Front Pediatr
Specialty Pediatrics
Date 2016 May 21
PMID 27200326
Citations 4
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Abstract

C3 glomerulopathy is an umbrella term, which includes several rare forms of glomerulonephritis (GN) with underlying defects in the alternate complement cascade. A common histological feature noted in all these GN is dominant C3 deposition in the glomerulus. In this review, we will provide an overview of the complement system as well as mediators, with an introduction to pharmaceutical agents that can alter the pathway.

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References
1.
Rabasco C, Cavero T, Roman E, Rojas-Rivera J, Olea T, Espinosa M . Effectiveness of mycophenolate mofetil in C3 glomerulonephritis. Kidney Int. 2015; 88(5):1153-60. DOI: 10.1038/ki.2015.227. View

2.
McGinley E, Watkins R, McLay A, Boulton-Jones J . Plasma exchange in the treatment of mesangiocapillary glomerulonephritis. Nephron. 1985; 40(4):385-90. DOI: 10.1159/000183504. View

3.
Jokiranta T, Solomon A, Pangburn M, Zipfel P, Meri S . Nephritogenic lambda light chain dimer: a unique human miniautoantibody against complement factor H. J Immunol. 1999; 163(8):4590-6. View

4.
Licht C, Heinen S, Jozsi M, Loschmann I, Saunders R, Perkins S . Deletion of Lys224 in regulatory domain 4 of Factor H reveals a novel pathomechanism for dense deposit disease (MPGN II). Kidney Int. 2006; 70(1):42-50. DOI: 10.1038/sj.ki.5000269. View

5.
Noris M, Remuzzi G . Atypical hemolytic-uremic syndrome. N Engl J Med. 2009; 361(17):1676-87. DOI: 10.1056/NEJMra0902814. View