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Table 4 Serum ceruloplasmin levels in WD children carrying R778L mutation

From: Assessment of the diagnostic value of serum ceruloplasmin for Wilson’s disease in children

Genotype

Age (years)

Cp (mg/dL)

No. of patients

Total

0–5

5–10

10–15

15–20

≥ 20

R778L homozygotes

5.7 ± 3.1

2.3 ± 0.5*

9

9

0

0

0

0

R778L heterozygotes

6.2 ± 3.0

5.2 ± 4.5

97

64

21

6

3

3

No R778L

6.1 ± 2.8

6.1 ± 4.8

207

108

57

29

10

3

Total

6.1 ± 2.9

5.7 ± 4.7

313

181

78

35

13

6

  1. WD, Wilson’s disease; Cp, ceruloplasmin
  2. *Represents statistical significance of serum ceruloplasmin between WD children with and without R778L, p value < 0.05