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. 2021 Feb 15;11:3844. doi: 10.1038/s41598-021-82297-y

Table 2.

Distribution of hemoglobin fractions presented in 169 α-thalassemia fetuses (%).

Genotype N (cases) HbF HbA HbA2 Hb Barts Hb CS HbF variant Hb Portland Hb Epsilon4 Hb Gower1 HbH
α-thalassemia α-thalassemia silent carrier (one alpha-gene defect) 15 91.49 ± 3.01 7.74 ± 2.69 0.1 (1 case) 0.81 ± 0.66
α-thalassemia trait (two alpha-gene defects) 31 83.75 ± 9.88 9.46 ± 3.71 0.3 ± 0.08 (4 cases) 4.71 ± 2.81 1.10–2.50 (2 cases) 5.70–54.90 (2 cases) 1.30 (1 case)
α-thalassemia intermedia (three alpha-gene defects) 21 61.76 ± 10.13 11.62 ± 3.46 0.20–0.40 (2 cases) 23.52 ± 5.63 1.50 ± 0.56 (4 cases) 46.20 (1 case) 0.74 ± 0.17 (10 cases) 0.52 ± 0.17 (9 cases) 0.20
α-thalassemia major (four alpha-gene defects) 102 86.02 ± 3.79 12.33 ± 1.72 (3 cases) 11.67 ± 3.0 1.55 ± 0.21 (39 cases) 4.20 ± 2.15 (39 cases) 0.91 ± 0.44 (26 cases)