33 Scopus citations


Alpha1-antitrypsin deficiency is the most common genetic cause of liver disease in infants and children and is the most common genetic disease for which liver transplantation is indicated. This article presents the clinical manifestations, diagnosis, treatment, and pathogenesis of alpha1-antitrypsin deficiency.

Original languageEnglish
Pages (from-to)27-43
Number of pages17
JournalGastroenterology Clinics of North America
Issue number1
StatePublished - Jan 1 1995


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