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Hereditary spherocytosis concomitant with JAK2V617F-positive primary myelofibrosis: a case report

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Hereditary spherocytosis (HS) is a genetic hemolytic disorder primarily characterized by hemolytic anemia, jaundice, splenomegaly, and frequent complications, including cholelithiasis, accompanied by the presence of spherocytes in the peripheral blood. This di... ...