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Results 1 - 10 of 14 for Familial hemolytic anemia
  1. Pyruvate kinase deficiency 
    ... is the most common inherited cause of nonspherocytic hemolytic anemia. More than 500 affected families have been identified, and studies suggest that the ...
    https://medlineplus.gov/.../condition/pyruvate-kinase-deficiency - Genetics
  2. Hereditary spherocytosis 
    ... with no history of the disorder in their family.This condition can also be inherited in an autosomal ... ...
    https://medlineplus.gov/genetics/condition/hereditary-spherocytosis - Genetics
  3. Thrombotic thrombocytopenic purpura 
    ... blood cells can break apart. A condition called hemolytic anemia occurs ... form and a familial (inherited) form. The acquired form usually appears in ...
    https://medlineplus.gov/.../thrombotic-thrombocytopenic-purpura - Genetics
  4. SLC4A1 gene 
    ... below). The blood cell abnormalities can lead to hemolytic anemia, in which the abnormal red blood cells are ... these abnormal red blood cells may lead to hemolytic anemia. More About This Health Condition Mutations in the ...
    https://medlineplus.gov/genetics/gene/slc4a1 - Genetics
  5. 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
  6. STAT3 gene 
    ... pancreas (type 1 diabetes), red blood cells (autoimmune hemolytic anemia), platelets (autoimmune thrombocytopenia), or tissues in the digestive ... an autoimmune disorder, primarily rheumatoid arthritis or autoimmune hemolytic anemia, and other blood cell abnormalities, such as pure ...
    https://medlineplus.gov/genetics/gene/stat3 - Genetics
  7. 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
  8. Phosphoglycerate kinase deficiency 
    ... is characterized by a condition known as chronic hemolytic anemia, in which red blood cells are broken down (undergo hemolysis) prematurely. Chronic hemolytic anemia can lead to unusually pale skin (pallor), yellowing ...
    https://medlineplus.gov/.../phosphoglycerate-kinase-deficiency - Genetics
  9. Autoimmune lymphoproliferative syndrome 
    ... immune system may attack red blood cells (autoimmune hemolytic anemia), white blood cells (autoimmune neutropenia), or platelets (autoimmune ... years later, most frequently as a combination of hemolytic anemia and thrombocytopenia, also called Evans syndrome. People with ...
    https://medlineplus.gov/.../autoimmune-lymphoproliferative-syndrome - Genetics
  10. Paroxysmal nocturnal hemoglobinuria 
    ... a shortage of these cells in the blood (hemolytic anemia), which can cause signs and symptoms such as ... red blood cells are prematurely destroyed, leading to hemolytic anemia. Studies show that GPI anchors with no attached ...
    https://medlineplus.gov/.../paroxysmal-nocturnal-hemoglobinuria - Genetics
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