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hemoglobinopathy

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hemoglobinopathy

Any of a group of disorders caused by genetic abnormality of the hemoglobin molecule. The most prominent types are sickle-cell anemia and thalassemia, a set of disorders whose symptoms range from none to fatal anemia.


hemoglobinopathy [‚hē·mə‚glō·bə′näp·ə·thē]
(medicine)
Any blood dyscrasia resulting from the genetically determined alteration of the chemical nature of hemoglobin.


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The first patient was a 63-year-old woman with hemoglobin AEBart's disease, a complex thalassemia/ hemoglobinopathy syndrome, which required frequent blood transfusions.
hemoglobinopathy, gout, Waldenstrom's Macroglobulinemia).
The patient was a 31-year-old woman, who had undergone splenectomy at age 9 years, for severe double heterozygous hemoglobinopathy (beta-thalassemia and hemoglobin E disease).
 
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