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Updated: Mar 30, 2026

Methods for Quantitative Detection of Antibody-induced Complement Activation on Red Blood Cells
Published on: January 29, 2014
Coexistence of immunoglobulin M nephropathy and autoimmune hemolytic anemia: 2 rare entities
Nergiz Bayrakci1, Nihal Ozkayar, Muge Erek Ersozen
1Department of Nephrology, Ankara Numune Education and Research Hospital, Ankara, Turkey. nrgzbayrakci@yahoo.com.
Abstract:
Immunoglobulin M (IgM) nephropathy is described as mesengial proliferative glomerulonephritis with diffuse mesengial IgM deposition. We report a patient diagnosed with IgM nephropathy and concomitant autoimmune hemolytic anemia syndrome associated with cold-reacting autoantibodies. Complete remission was achieved with systemic corticosteroid and plasmapheresesis.
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