Hemoglobinopathies

The word hemoglobinopathy refers to a number of inherited disorders that result from mutations in the globin (alpha, beta, or gamma) genes. These mutations result in either condensed production or altered structure of the hemoglobin (Hb) molecule.
The hemoglobinopathies are a group of disorders delivered down through families (inherited) in which there is abnormal production or structure of the hemoglobin molecule. This group of disorders includes

  • Hemoglobin C disease
  • Hemoglobin S-C disease
  • Sickle cell anemia
  • Thalassemias
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