Hemolytic anemia or haemolytic anaemia is a form of anemia due to hemolysis, the abnormal breakdown of red blood cells (RBCs), either in the blood vessels...
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Microangiopathic hemolytic anemia (MAHA) is a microangiopathic subgroup of hemolytic anemia (loss of red blood cells through destruction) caused by factors...
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Autoimmune hemolytic anemia (AIHA) is an autoimmune disorder which occurs when antibodies directed against the person's own red blood cells (RBCs) cause...
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Congenital hemolytic anemia (CHA) is a diverse group of rare hereditary conditions marked by decreased life expectancy and premature removal of erythrocytes...
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autoimmune hemolytic anemia, hemolysis secondary to drug toxicity, thalassemia minor, and congenital dyserythropoietic anemias. Pathophysiology of hemolytic jaundice...
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Mechanical hemolytic anemia is a form of hemolytic anemia due to mechanically induced damage to red blood cells. Red blood cells, while flexible, may in...
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of anemia treated with drugs are iron-deficiency anemia, thalassemia, aplastic anemia, hemolytic anemia, sickle cell anemia, and pernicious anemia, the...
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Warm antibody autoimmune hemolytic anemia (WAIHA) is the most common form of autoimmune haemolytic anemia. About half of the cases are of unknown cause...
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Wayback Machine at Mount Sinai Hospital [1] at Mount Sinai Hospital "Hemolytic Anemia: Overview - eMedicine Hematology". Retrieved 2009-02-07. "Beta thalassemia"...
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Kernicterus Neutropenia Thrombocytopenia Hemolytic anemia – must not be treated with iron Late onset anemia – must not be treated with iron. Can persist...
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Acquired hemolytic anemia can be divided into immune and non-immune mediated forms of hemolytic anemia. Autoimmune hemolytic anemia Warm antibody autoimmune...
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Drug-induced autoimmune hemolytic anemia also known as Drug-induced immune hemolytic anemia (DIIHA) is a rare cause of hemolytic anemia. It is difficult to...
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blood clotting), and destruction of red blood cells (microangiopathic hemolytic anemia). High blood pressure, jaundice (a yellow tinge in skin and the whites...
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elliptocytosis and schistocytes for intravascular hemolysis. Many hemolytic anemias show multiple poikilocytes such as G6PD deficiency, which may show...
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Sickle cell disease (redirect from Sickle Cell Anemia)
Fibach E, Rachmilewitz E (2008). "The Role of Oxidative Stress in Hemolytic Anemia". Current Molecular Medicine. 8 (7): 609–619. doi:10.2174/156652408786241384...
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Hereditary spherocytosis (redirect from Congenital spherocytic hemolytic anemia)
the spleen, which leads to a shortage of erythrocytes and results in hemolytic anemia. HS was first described in 1871, and is the most common cause of inherited...
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Cold agglutinin disease (redirect from Cold agglutinin hemolytic anemia)
them to agglutinate and undergo lysis. It is a form of autoimmune hemolytic anemia, specifically one in which antibodies bind red blood cells only at...
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Schistocyte (section Hemolytic-uremic syndrome)
often seen in patients with hemolytic anemia. They are frequently a consequence of mechanical artificial heart valves, hemolytic uremic syndrome, and thrombotic...
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Cold autoimmune hemolytic anemia caused by cold-reacting antibodies. Autoantibodies that bind to the erythrocyte membrane leading to premature erythrocyte...
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Kernicterus Neutropenia Thrombocytopenia Hemolytic Anemia - MUST NOT be treated with iron Late onset anemia - Must NOT be treated with iron. Can persist...
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Glucose-6-phosphate dehydrogenase deficiency (redirect from Hereditary non-spherocytic hemolytic anemia)
G6PD/NADPH/glutathione. People with G6PD deficiency are therefore at risk of hemolytic anemia in states of oxidative stress. Oxidative stress can result from infection...
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Reduced kidney function Hemolytic anemia (microangiopathic hemolytic anemia). TTP, as with other microangiopathic hemolytic anemias (MAHAs), is caused by...
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Thalassemia (redirect from Mediterranean Anemia)
populations, hemoglobin C/βo thalassemia causes a moderately severe hemolytic anemia with splenomegaly; hemoglobin C/β+ thalassemia produces a milder disease...
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Paroxysmal cold hemoglobinuria (redirect from Donath–Landsteiner hemolytic anemia)
cold hemoglobinuria (PCH) or Donath–Landsteiner hemolytic anemia (DLHA) is an autoimmune hemolytic anemia featured by complement-mediated intravascular...
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Conditions where this is found include aplastic, posthemorrhagic, and hemolytic anemias and anemia of chronic disease. MCH (average amount of hemoglobin found in...
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Mixed autoimmune hemolytic anemia (MAIHA) is a type of autoimmune hemolytic anemia which combines the features of cold sensitive antibody-induced diseases...
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Spur cell hemolytic anemia, Chronic liver disease impairs the liver's ability to esterify cholesterol, causing free cholesterol to bind to the red cell...
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Spherocytosis (category Anemias)
Spherocytes are found in all hemolytic anemias to some degree. Hereditary spherocytosis and autoimmune hemolytic anemia are characterized by having only...
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used to test for autoimmune hemolytic anemia, a condition where the immune system breaks down red blood cells, leading to anemia. The direct Coombs test is...
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