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Results 1 - 5 of 5 for Hereditary persistence of fetal hemoglobin
  1. Beta thalassemia is a blood disorder that reduces the production of hemoglobin. Hemoglobin is the iron-containing protein ... to cells throughout the body.In people with beta thalassemia, low levels of hemoglobin reduce oxygen levels in ...
  2. ... also called mutations) have been found to cause beta thalassemia. Most of the variants involve a change in ... organ damage, and other health problems associated with beta thalassemia. More About This Health Condition Variants in the ...
  3. ... levels of beta-globin; this condition is called beta thalassemia.In people with sickle cell disease, at least ... If the variants that produce hemoglobin S and beta thalassemia occur in the same individual, that individual will ...
  4. ... and thrombocytopenia have additional blood disorders such as beta thalassemia or congenital erythropoietic porphyria. Beta thalassemia is a condition that reduces the production of ...
  5. ... corpus callosum with peripheral neuropathy Polycystic kidney disease Beta thalassemia Bloom syndrome Canavan disease PMM2 -congenital disorder of ...