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beta Thalassemia
- Beta thalassemia is a blood disorder that reduces the production of hemoglobin. Hemoglobin is the iron-containing protein in red blood cells that carries ...
- ... protein are missing or there is a variant. Beta thalassemia occurs when similar gene defects affect production of ... type has many different subtypes. Both alpha and beta thalassemia include the following two forms: Thalassemia major Thalassemia ...
- ... chest pain, and stroke) or with transfusion-dependent beta thalassemia (TDT; inherited blood disorder where body does not product enough beta globin, required to make hemoglobin, so blood transfusions ...
- ... people who require regular blood transfusions to treat beta thalassemia (Cooley's anemia; an inherited condition that causes a ...
- ... 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 ...
- ... 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 ...
- Thalassemia (National Library of Medicine)Thalassemias are inherited blood disorders. If you have one, your body makes fewer healthy red blood cells and less hemoglobin. Hemoglobin is a protein that carries ...
- ... and thrombocytopenia have additional blood disorders such as beta thalassemia or congenital erythropoietic porphyria. Beta thalassemia is a condition that reduces the production of ...
- Thalassemia
- beta-thalassemia.html (Nemours Foundation)Thalassemia