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Gastroenterol Clin North Am. 1995 Mar;24(1):27-43.

Clinical manifestations of alpha 1-antitrypsin deficiency.

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  • Washington University School of Medicine, St. Louis, Missouri, USA.

Abstract

Alpha 1-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 alpha 1-antitrypsin deficiency.

PMID:
7729860
[PubMed - indexed for MEDLINE]
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