Hereditary elliptocytosis

Hereditary elliptocytosis (HE) is a rare clinically and genetically heterogeneous disorder of the red cell membrane characterized by manifestations ranging from mild to severe transfusion-dependent hemolytic anemia but with the majority of patients being asymptomatic.

Also known as: HE, Hashimoto Encephalopathy, congenital elliptocytosis, hereditary ovalocytosis, ovalocytosis

42 clinical trials for this condition and its sub-types.