hemolytic anemias การใช้

• Aldolase A deficiency has been associated with myopathy and hemolytic anemia.
• The most common clinical manifestations are neonatal jaundice and acute hemolytic anemia.
• These include : Autoimmune hemolytic anemia, Autoimmune neutropenia, Autoimmune thrombocytopenia.
• It has not been associated with autoimmune hemolytic anemia of the fetus.
• RA may also cause a warm autoimmune hemolytic anemia.
• Schistocytes are often seen in patients with hemolytic anemia.
• Individuals with cold agglutinin disease present with signs and symptoms of hemolytic anemia.
• In the case of hemolytic anemia, PGK deficiency occurs in the erythrocytes.
• It is a potential cause of neonatal hemolytic anemia.
• In general, hemolytic anemia occurs as a modification of the RBC life cycle.
• In autoimmune hemolytic anemia, concentrations of hemoglobin A1 ( HbA1 ) is undetectable.
• Its overall pathology resembles a combination of autoimmune hemolytic anemia and immune thrombocytopenic purpura.
• Horses have developed hemolytic anemia from ingesting wild onion leaves ( Scoggan 1989 ).
• Deficiency of gamma-glutamylcysteine synthetase in human is associated with enzymopathic hemolytic anemia.
• This includes : aplastic, posthemorrhagic, and hemolytic anemias and anemia of chronic disease.
• Examples include red blood cells in autoimmune hemolytic anemia and acetylcholine receptors in myasthenia gravis.
• Hemolytic anemia occurs when red blood cells are destroyed faster than the body can replace them.
• People with G6PD deficiency are therefore at risk of hemolytic anemia in states of oxidative stress.
• It is characterized by hemolytic anemia and neurodegeneration, and is caused by anaerobic metabolic dysfunction.
• It is a congenital disease that most often occurs with hemolytic anemia and manifests with jaundice.