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Article

[Pathogenesis of liver disease in alpha 1-antitrypsin deficiency].

Acta medica Austriaca - 1 Jan 1990

Vogel W, Braunsteiner T, Dietze O, Braunsteiner H

Abstract excerpt

Alpha-1-antitrypsin deficiency (A1ATD) is one of the most common lethal hereditary disorders. Approximately 5 to 10% of the general population carry an "at risk" gene for the development of liver disease or emphysema of the lung. Patients with A1ATD associated liver disease constitute a histologi...

Topics

Genetic Carrier Screening
Humans
Liver Cirrhosis
Liver Diseases
Mutation
Phenotype
alpha 1-Antitrypsin
alpha 1-Antitrypsin Deficiency

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 2092568

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-2092568-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

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