Hemoglobin A2 (Hgb A2) values of 3.5% to 9% are found in beta-thalassemia trait.
In beta-thalassemia major, hemoglobin F (Hgb F) may be 30% to 90% or even more of the total hemoglobin.
Hgb F concentration is usually between 5% to 15% of the total hemoglobin in delta/beta-type thalassemia trait (F-thalassemia).
Higher concentrations of Hbg F occur in hemoglobin S (Hgb S)/beta zero-thalassemia, in patients who are doubly heterozygous for the Hgb S gene, and in patients who have a gene for hereditary persistence of fetal hemoglobin (HPFH). These disorders may be differentiated by family studies or by flow cytometry studies for Hgb F (HPFH/8270 Hemoglobin F, Red Cell Distribution, Blood), which reveals uniform intraerythrocytic distribution of Hgb F in HPFH and nonuniform distribution in Hgb S/beta thalassemia.
The electrophoretic finding of small quantities of Hgb A in a patient who has mostly Hgb S and a moderate increase in Hgb F is strong evidence of Hgb S/beta thalassemia (if the patient has not had a transfusion).
Hgb F values greater than normal (2%) may be seen in chronic anemias, beta-thalassemia, and HPFH