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hereditary elliptocytosis

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hereditary elliptocytosis

Hereditary ovalocytosis Hematology An AD condition, affecting ±1:2500 of the general population; 15% of the RBCs are ovoid; hemolysis is uncommon, but severe in 5%
McGraw-Hill Concise Dictionary of Modern Medicine. © 2002 by The McGraw-Hill Companies, Inc.
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Hereditary elliptocytosis: spectrin and protein 4.1 R.
Hereditary elliptocytosis is caused by mutations in in structural components of the erythrocyte cell membrane.
It can be positive in hereditary elliptocytosis and autoimmune hemolytic anemia.
Hereditary spherocytosis RBC spectrin RBC ankyrin Hereditary elliptocytosis RBC spectrin Hereditary pyropoikilocytosis RBC spectrin Hemolytic anemia - Glucose- G-6-PD 6-phosphate dehydrogenase deficiency Hereditary nonspherocytic PDH hemolytic anemia - Pyruvate kinase deficiency Porphyrias Various genes encoding enzymes of the heme biosynthesis pathway
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