Atypical hemolytic-uremic syndrome due to complement factor I mutation

doi:10.5527/wjn.v6.i6.243

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Nov 6, 2017 (publication date) through Jan 4, 2025

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World Journal of Nephrology

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2220-6124

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

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World J Nephrol. Nov 6, 2017; 6(6): 243-250
Published online Nov 6, 2017. doi: 10.5527/wjn.v6.i6.243

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Figure 1 Finding of renal biopsy showed. A: A glomerulus with extensive fibrin thrombi involvement, obliterating the capillary loops (Periodic Acid-Schiff stain, original magnification × 400); B: A glomerulus with an afferent arteriole with extensive red, fuchsinophilic material (fibrin) involvement (Masson trichrome stain, original magnification × 400); C: A small arteriole with luminal fibrin staining red (fuchsinophilic) (Masson trichrome stain, original magnification × 400).

Citation: Almalki AH, Sadagah LF, Qureshi M, Maghrabi H, Algain A, Alsaeed A. Atypical hemolytic-uremic syndrome due to complement factor I mutation. World J Nephrol 2017; 6(6): 243-250
URL: https://www.wjgnet.com/2220-6124/full/v6/i6/243.htm
DOI: https://dx.doi.org/10.5527/wjn.v6.i6.243