From: Mutation spectrum and biochemical features in infants with neonatal Dubin-Johnson syndrome
Diagnosis | N = 135 |
---|---|
Biliary atresia | 37 (27.4%) |
Choledochal cyst | 11 (8.1%) |
NICCD | 7 (5.2%) |
Dubin Johnson syndrome | 6 (4.5%) |
TPN induced cholestasis | 6 (4.5%) |
Alagille syndrome | 4 (3.0%) |
Neonatal hemochromatosis | 2 (1.5%) |
ARC syndrome | 2 (1.5%) |
Congenital portosystemic shunt | 2 (1.5%) |
PFIC | 1 (0.7%) |
Galactosemia | 1 (0.7%) |
HSV | 1 (0.7%) |
CMV | 1 (0.7%) |
Sepsis | 1 (0.7%) |
Idiopathic neonatal cholestasis | 53 (39.3%) |