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Table 2 The hematological datas of individuals with the main genotype shown in Fig. 1

From: Molecular epidemiology and hematologic characterization of δβ-thalassemia and hereditary persistence of fetal hemoglobin in 125,661 families of greater Guangzhou area, the metropolis of southern China

cases

Hb (g/dL)

MCV (fL)

MCH (pg)

HbA (%)

HbA2 (%)

HbF(%)

Genotype

77(F:49, M:28)

135.2 ± 14.9

70.6 ± 7.0

24.9 ± 15.3

82.0 ± 2.6

2.4 ± 0.3

15.5 ± 2.6

Chinese Gγ (Aγδβ)0N

8 (F:1, M:7)

129.9 ± 8.37

69.1 ± 3.4

22.5 ± 1.4

86.8 ± 2.5

2.5 ± 0.2

10.6 ± 2.4

Chinese Gγ (Aγδβ)0combined with --SEA/αα

1(M)

155

77.9

24.1

86.1

2.7

1.2

Chinese Gγ (Aγδβ)0combined with -α3.7/αα

1(F)

126

81

26

82.1

2

15.9

Chinese Gγ (Aγδβ)0combined with -α4.2/αα

1(M)

137

74.7

23.1

83.6

2.7

13.7

Chinese Gγ (Aγδβ)0 combined withααWS/αα

1(M)

128

64.8

20.3

16.0

2.7

81.3

Chinese Gγ (Aγδβ)0−28

50(F:23,M:27)

137.8 ± 14.0

76.6 ± 4.3

25.1 ± 1.5

74.2 ± 4.2

4.0 ± 0.6

21.8 ± 4.8

SEA-HPFH/βN

3(F:1,M:2)

130.0 ± 11.1

69.5 ± 0.6

22.2 ± 0.2

76.4 ± 4.1

3.7 ± 0.5

19.9 ± 4.1

SEA-HPFH/βN combined with --SEA/αα

5(F:2,M:3)

115.33 ± 23.75

66.73 ± 6.02

20.53 ± 2.76

86.26 ± 2.63

6.83 ± 0.57

6.9 ± 3.1

Taiwanese deletion/βN

37(F:15,M:22)

147.8 ± 14.6

88.7 ± 5.0

29.6 ± 2.1

85.0 ± 1.4

1.8 ± 0.2

14.9 ± 2.3

Aγ-196 C-T mutation

14(F:7,M:7)

128.3 ± 18.9

68.3 ± 4.2

21.7 ± 1.2

83.4 ± 2.4

1.4 ± 0.1

13.8 ± 1.5

Aγ-196 C-T mutation combined with --SEA/αα

1(F)

117

69.2

22.1

70

4.1

25.9

Aγ-196C-T mutation combined with --SEA/αα and β−28N

1(F)

114

67.7

21.4

70

1.6

16.6

Homozygote for Aγ-196C-T mutation combined with --SEA/αα

1(M)

163

84

29.4

82.2

2.3

15.5

Homozygote for Aγ-196C-T mutation

1(M)

148

72.4

23.1

88.8

2.1

9.1

Aγ-197 C-T mutationcombined with --SEA/αα

1(F)

108

72.8

23.8

77.2

2.3

11.30

Hb Lepore-Boston/Washington