Hemoglobin C disease

Abstract:
Hemoglobin C disease belongs to the hemoglobinopathies. It occurs in inhabitants of western Africa and their descendants. A diagnosis is established by blood film examination and hemoglobin electrophoresis.

Clinical picture:
Only the homozygous form of hemoglobin C is symptomatic. Anemia is not severe with values between 80 and 120 g/L. A mild hemolysis and a palpable splenomegaly occur.

Hematology:
Typically, up to 80% of the erythrocytes are target cells. Additionally, a polychromasia often occurs as well as hypochromia and microcytosis in some patients.


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