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Table 3 The genotypes of G6PD deficiency and bilirubin level in jaundiced neonates

From: Co-inheritance of G6PD deficiency and 211 G to a variation of UGT1A1 in neonates with hyperbilirubinemia in eastern Guangdong

Type of mutation

M*

(n)

F*

(n)

Proportion

(%)

Total bilirubin

(μmol/L)

Cases number in different postnatal days

 

<1d

<2d

<3d

<4d

<5d

<6d

<7d

7-14d

14-28d

c.1376G > T(Canton)

31

3

45.95

312.60 ± 71.81

0

1

2

7

5

7

2

5

5

c.1388G > A(Kaiping)

25

1

35.14

367.88 ± 75.79

1

1

4

4

3

3

1

6

3

c.95A > G(Gaohe)

2

0

2.70

428.95 ± 168.22

0

0

0

0

0

1

0

1

0

c.392G > T(Qing Yan)

2

0

2.70

264.64 ± 93.52

0

0

0

1

0

0

0

1

0

c.487G > A(Mahidol)

1

0

1.35

332

0

0

0

0

0

1

0

0

0

c.1024C > T(Chinese-5)

1

0

1.35

306

0

0

0

0

1

0

0

0

0

c.1311C > T

1

0

1.35

318.3

0

0

0

0

0

0

0

0

1

c.1311C > T/

c.871 G > A (Viangchan)

1

1

2.70

418.6

0

0

0

0

0

1

0

0

1

c.1388G > A/

c.95A > G

0

1

1.35

280.1

0

0

0

0

0

0

0

0

1

Unidentified

3

1

5.41

319.65 ± 69.55

0

0

0

0

1

0

1

2

0

Total

67

7

100

334.43 ± 79.27

1

2

6

12

10

13

4

15

11

  1. M* Male, F* Female