A hemoglobinopathy is a genetic disorder which alters the structure of hemoglobin 1. The result is reduced oxygen-carrying capacity of the blood to the tissues.

Types of hemoglobinopathies include the following:

  • sickle cell disease (Hb S)
  • sickle cell trait (HB AS)
  • sickle cell-hemoglobin C (Hb S-C)
  • sickle cell-thalassemia (Hb S and Hb A)
  • thalassemia
    • alpha thalassemia (deficient alpha-globin chain synthesis)
    • beta thalassemia (deficient beta-globin chain synthesis)
      • thalassemia major (homozygous) - Cooley anemia
      • thalassemia minor (heterozygous)
  • hemoglobin C disease (Hb CC)
  • hemoglobin C trait (Hb AC)

Clinical presentation varies, is related to hypoxia, and characteristically includes the following:

  • claudication
  • tachycardia
  • dyspnea
  • vertigo
  • angina
  • vascular occlusion leading to infarcts
  • necrosis
  • pathological fracture
  • osteomyelitis (100x more likely in sickle cell disease patients) 2

The radiographic features of hemoglobinopathies vary and are generally related to extramedullary hematopoiesis and infarctions as follows:

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Article information

rID: 50963
System: Haematology
Section: Syndromes
Synonyms or Alternate Spellings:
  • Hemoglobinopathies
  • Hemoglobinopathy

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