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Article detail · 2023

Two Different Presentation of C3 Glomerulonephritis Treated with Eculizumab: Two Cases and Brief Overview

Turkish Journal of Nephrology

YÖKSİS OpenAlex Open access · diamond SJR Q4 JCR Q4 TR Index Citations 0 Percentile 15.4% FWCI 0.0
Year
2023
ISSN
2667-4440
Type
article

Data source split

  • YÖKSİS YÖKSİS article record
  • OpenAlex OpenAlex enrichment (abstract, citations, topics)

Abstract

English (OpenAlex)

C3 glomerulopathy (C3 GP) is a newly-defined glomerular disease dominated by C3 complement storage and uncertain C1, C4 and immunoglobin accumulations. Hereditary mutations associated with CFH causing hyperactivation of the alternative complement pathway were identified. Most mutations associated with C3 GP are associated with the N-terminal end. Whether mutations are pathogenic or not will direct diagnosis and treatment. We present two cases, one 61-years-old and one 24-years-old attending our clinic at different times with hematuria, proteinuria, edema and kidney failure. Both patients had C3 glomerulopathy diagnosed based on the results of kidney biopsy and were treated with eculizumab. Both cases had CFH-associated mutations. Cite this article as: Öztürk Y, Özer H, Baloğlu İ, Türkmen K. Two different presentation of C3 glomerulonephritis treated with eculizumab: Two cases and brief overview. Turk J Nephrol. 2023;32(1):86-89.

Topics

  • Complement system in diseases
  • Amyloidosis: Diagnosis, Treatment, Outcomes
  • Coagulation, Bradykinin, Polyphosphates, and Angioedema

Primary topic Complement system in diseases

Authors

  1. YASİN ÖZTÜRK ZONGULDAK BÜLENT ECEVİT ÜNİVERSİTESİ
  2. HAKAN ÖZER İZMİR BAKIRÇAY ÜNİVERSİTESİ
  3. İSMAİL BALOĞLU NECMETTİN ERBAKAN ÜNİVERSİTESİ
  4. KÜLTİGİN TÜRKMEN