Clinical manifestations of alpha 1-antitrypsin deficiency.

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.

authors

Perlmutter DH

subject

Has Abstract

pub_date

1995-03-01 00:00:00

pages

27-43

issue

1

eissn

0889-8553

issn

1558-1942

journal_volume

24

pub_type

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