Skip to main content

Table 2 Criteria used in diagnosis of WD in the studied group

From: Phenotypic and Genetic Characterization of a Cohort of Pediatric Wilson Disease Patients

  

No.

%

S. Ceruloplasmin (mg%)

7

57/77

74

 

7-20

15/77

19.5

 

> 20

5/77

6.5

Positive Family history

56/72

77.8

K F ring

45/65

69.2

Elevated urinary copper excretion

19/25

84.2

Liver biopsy suggestive of WD

15/39

38.5

Coomb's negative hemolytic anemia

4/74

5.4