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Results 1 - 10 of 20 for Hemolytic anemia
  1. Pyruvate kinase deficiency 
    ... this disorder have a condition known as chronic hemolytic anemia, in which red blood cells are broken down ( ... a common cause of a type of inherited hemolytic anemia called hereditary nonspherocytic hemolytic anemia. In hereditary nonspherocytic ...
    https://medlineplus.gov/.../condition/pyruvate-kinase-deficiency - Genetics
  2. Hereditary spherocytosis 
    ... signs and symptoms of the condition. Congenital spherocytic hemolytic anemia Congenital spherocytosis HS Spherocytic anemia Spherocytosis, type 1 ...
    https://medlineplus.gov/genetics/condition/hereditary-spherocytosis - Genetics
  3. Glucose phosphate isomerase deficiency 
    ... this disorder have a condition known as chronic hemolytic anemia, in which red blood cells are broken down ( ... a shortage of red blood cells (anemia). Chronic hemolytic anemia can lead to unusually pale skin (pallor), yellowing ...
    https://medlineplus.gov/.../glucose-phosphate-isomerase-deficiency - Genetics
  4. SLC4A1-associated distal renal tubular acidosis 
    ... severity from no symptoms to a condition called hemolytic anemia, in which red blood cells prematurely break down ( ... causing a shortage of red blood cells (anemia). Hemolytic anemia can lead to unusually pale skin (pallor), extreme ...
    https://medlineplus.gov/...-associated-distal-renal-tubular-acidosis - Genetics
  5. Triosephosphate isomerase deficiency 
    ... red blood cells (hemolysis), it is known as hemolytic anemia. A shortage of red blood cells to carry ... the condition. Deficiency of phosphotriose isomerase Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency TPI deficiency TPID ...
    https://medlineplus.gov/.../triosephosphate-isomerase-deficiency - Genetics
  6. Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome 
    ... fatal infection syndrome, X-linked Enteropathy, autoimmune, with hemolytic anemia and polyendocrinopathy IDDM-secretory diarrhea syndrome Immunodeficiency, polyendocrinopathy, ...
    https://medlineplus.gov/...ocrinopathy-enteropathy-x-linked-syndrome - Genetics
  7. Glucose-6-phosphate dehydrogenase deficiency 
    ... associated with glucose-6-phosphate dehydrogenase deficiency is hemolytic anemia, which occurs when red blood cells are destroyed ... In people with glucose-6-phosphate dehydrogenase deficiency, hemolytic anemia is most often triggered by bacterial or viral ...
    https://medlineplus.gov/...cose-6-phosphate-dehydrogenase-deficiency - Genetics
  8. Glutathione synthetase deficiency 
    ... results in the destruction of red blood cells (hemolytic anemia). In addition, affected individuals may release large amounts ... may experience symptoms beginning shortly after birth including hemolytic anemia, 5-oxoprolinuria, and elevated acidity in the blood ...
    https://medlineplus.gov/.../glutathione-synthetase-deficiency - Genetics
  9. Sitosterolemia 
    ... cells (anemia). This type of anemia is called hemolytic anemia. Affected individuals sometimes have abnormally shaped red blood ... membranes stiff and prone to rupture, leading to hemolytic anemia. Changes in the lipid composition of the membranes ...
    https://medlineplus.gov/genetics/condition/sitosterolemia - Genetics
  10. Atypical hemolytic-uremic syndrome 
    ... by three major features related to abnormal clotting: hemolytic anemia, thrombocytopenia, and kidney failure.Hemolytic anemia occurs when red blood cells break down (undergo ...
    https://medlineplus.gov/.../atypical-hemolytic-uremic-syndrome - Genetics
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