Successful liver transplantation for Budd‐Chiari syndrome in a patient with paroxysmal nocturnal hemoglobinuria treated with the anti‐complement antibody eculizumab
Andrew L. Singer, Jamye E. Locke, Zoe A. Stewart, Bonnie E. Lonze, James P. Hamilton, Jennifer R. Scudiere, Robert A. Anders, Russell P. Rother, Robert A. Brodsky, Andrew M. Cameron – 27 April 2009 – Paroxysmal nocturnal hemoglobinuria (PNH) is a rare, acquired hemolytic anemia caused by somatic mutations in the phosphatidylinositol glycan‐complementation class A gene and the resulting absence of a key complement regulatory protein, CD59.