Intrinsic red blood cell defects |
Hemoglobinopathies (eg, sickle cell disease, thalassemias) |
Membrane defects (eg, hereditary spherocytosis, elliptocytosis) |
Enzyme deficiencies (eg, G6PD, pyruvate kinase deficiencies) |
Extrinsic hemolytic processes |
Autoimmune hemolytic anemia (AIHA)
|
Hypersplenism |
Systemic disease
|
Drugs and toxins* |
Microangiopathies
|
Mechanical damage (eg, artificial heart valves, Kasabach-Merritt phenomena) |
Wilson disease |
Combined mechanism (intrinsic and extrinsic) |
Paroxysmal nocturnal hemoglobinuria (PNH) |
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