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Title: Collagenofibrotic glomerulopathy in a kidney transplant recipient: A first report. Author: Jdiaa SS, Moeckel GW, Kfoury HM, Medawar WA, Abu-Alfa AK. Journal: Am J Transplant; 2021 May; 21(5):1948-1952. PubMed ID: 33206467. Abstract: Collagenofibrotic glomerulopathy (CG) is a rare disease characterized by the deposition of collagen type 3 fibrils in the glomeruli. Patients may have proteinuria, hematuria, and/or renal dysfunction. CG is considered a progressive disease with variable rates of progression. The definitive diagnosis is made by electron microscopy with the presence of characteristic subendothelial and mesangial curved, comma-like, banded collagen type 3 fibers of 40-65 nm periodicity. We are reporting the first case of CG in a kidney transplant recipient with kidney disease of unknown cause.[Abstract] [Full Text] [Related] [New Search]