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Table 5 Literature review on SDS-PAGE results of RBC membrane protein abnormalities in patients with HS (%)

From: Molecular diagnosis of hereditary spherocytosis by multi-gene target sequencing in Korea: matching with osmotic fragility test and presence of spherocyte

RBC membrane protein

Italy2[16]

(n = 87)

Italy1[9]

(n = 300)

USA2[6]

(n = 55)

USA1[29]

(n = 166)

Spain[30]

(n = 62)

Japan2*[31]

(n = 60)

Japan1[32]

(n = 47)

Korea[28]

(n = 27)

Band 3

23 (26)

158 (53)

10 (18)

38 (23)

0

(20)

15 (32)

3 (11)

Spectrin only

36 (41)

98 (33)

7 (13)

0

19 (31)

0

8 (15)

2 (7)

Ankyrin only

0

13 (4)†

0

0

4(6)

(7)

1 (2)

8 (30)

Spectrin/ankyrin

16 (18)

6 (11)

100 (60)

34 (55)

0

1 (2)

1 (4)

Other combination

–

–

–

–

–

–

15 (34)

–

4.2 protein

6 (7)

2 (1)

0

3 (2)

0

(45)

3 (6)

4 (15)

Undetected

6 (7)

29 (10)

32 (58)

25 (15)

5 (8)

(28)

4 (9)

9 (33)

  1. *Only % without the number of the patients was presented in this study
  2. †Including both Ankyrin only and Spectrin/ankyrin