Saudi Journal of Gastroenterology
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SPECIAL ARTICLE
Year : 1999  |  Volume : 5  |  Issue : 1  |  Page : 1-8

Alpha 1-antitrypsin deficiency and related liver disease


Department of Medicine, Malmo University Hospital, Malmo, Sweden

Correspondence Address:
Abdul-Nasser Elzouki
Department of Medicine, Malmo University Hospital, 205 02 Malmo
Sweden
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Source of Support: None, Conflict of Interest: None


PMID: 19864752

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α1 ,-antitrypsin (α1 AT) deficiency is a relatively common genetic cause of liver disease among Caucasians. It is an autosomal recessive disorder characterized by reduced serum levels of α1 AT, a 52-kD glycoprotein that functions as an antiprotease. The deficiency state is caused by mutations in the α1 AT gene on chromosome 14. α1 AT shows considerable genetic variability, having more than 75 genetic variants (Pi types). The PiZ allele is the most common deficiency variant. PiZZ homozygotes have 15-20% of the normal plasma levels of α1 AT. The deficiency is due to lack of secretion of Z α1 AT from the hepatocyte, where inclusions are formed in the endoplasmic reticulum. Homozygous α1 AT deficiency (PiZZ) is known to predispose to emphysema and chronic liver disease. This review outlines the clinical manifestations and treatment of α1 AT deficiency associated liver disease, focusing on recent advances in the pathogenic mechanism of liver disease in this genetic disorder.


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