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Native liver histologic findings in the two examples of children with recurrent hemolytic uremic syndrome (HUS) due to complement factor H gene (CFH) mutation. (A and C) Patient presented here; (B and D) patient 1. (A and B) Periductal fibrosis involving medium-sized bile ducts (hematoxylin and eosin stain, 50×). (C and D) Mild fibrosis of terminal hepatic venules (trichrome stain, 100×).
