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Thalassemia
Thalassemia is also known as thalassemia. It is a group of hereditary microcytic hemolytic anemias. Their common feature is that due to the defect of globin gene, one or several globin peptide chains in hemoglobin are reduced or cannot be synthesized. This leads to changes in the composition of hemoglobin. The clinical symptoms of this group of diseases vary in severity, and most of them manifest as chronic progressive hemolytic anemia.
  • Site of disease:

    Blood vessels
  • Infectious :

    Not contagious
  • Frequent population:

    All people, infants and young children
  • Related symptoms:

    Qi and blood deficiency Splenomegaly Dizziness Light yellow or dark golden skin Severe anemia
  • Concurrent disease:

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