Table 1.

Clinical and biochemical data obtained from the Wilsońs disease patients (n = 28).

Family screening	12 (42.8%)
Abnormal hepatic enzymes	5 (17.8%)
Symptoms of hepatitis	7 (25%)
Hepatosplenomegaly + neurological symptoms	3 (10.7%)
Fulminant hepatitis + hemolytic anemia (Coombs positive)	1 (3.5%)