TURKISH JOURNAL OF MEDICAL SCIENCES, cilt.50, sa.5, ss.1344-1349, 2020 (SCI-Expanded)
Background/aim: Paroxysmal nocturnal hemoglobinuria (PNH) is a very rare clonal hematopoietic stem cell disease characterized by chronic hemolytic anemia and thrombosis. We report data from a study of the occurrence of PNH among patients with idiopathic portal vein thrombosis (PVT).