Liver disease in children with pizz α1‐antitrypsin deficiency
Fayez K. Ghishan, Harry L. Greene – 1 March 1988 – We present our experience with 18 pediatric patients with α1‐antitrypsin deficiency of the PiZZ phenotype. Fifteen patients (83%) presented with neonatal cholestatic jaundice at a mean age of 2 ± 0.6 months (±S.D.). The male:female ratio was 15:3, indicating a male predominance. All metabolic, infectious and obstructive causes of jaundice were ruled out by appropriate tests in the patients with neonatal cholestasis.