Clinical manifestations of alpha1-antitrypsin deficiency

D. H. Perlmutter

Clinical manifestations of alpha₁-antitrypsin deficiency

D. H. Perlmutter

Research output: Contribution to journal › Review article › peer-review

Abstract

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 language	English
Pages (from-to)	27-43
Number of pages	17
Journal	Gastroenterology Clinics of North America
Volume	24
Issue number	1
State	Published - Jan 1 1995

Cite this

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title = "Clinical manifestations of alpha1-antitrypsin deficiency",

abstract = "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.",

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N2 - 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.

AB - 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.

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M3 - Review article

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AN - SCOPUS:0028924702

SN - 0889-8553

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JO - Gastroenterology Clinics of North America

JF - Gastroenterology Clinics of North America

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ER -

Clinical manifestations of alpha₁-antitrypsin deficiency

Abstract

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