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Article

Retrospective analysis of children with α-1 antitrypsin deficiency.

European journal of gastroenterology & hepatology - 1 Jul 2018

Comba Atakan, Demirbaş Fatma, Çaltepe Gönül, Eren Esra, Kalayci Ayhan G

Abstract excerpt

BACKGROUND: α-1 Antitrypsin (AAT) deficiency is the most frequently occurring genetic liver disorder. The association among classical α-1 antitrypsin deficiency (AATD), chronic liver disease, and cirrhosis is common in adult patients but rare in children. AIM: To assess the clinical characteristics of children with AATD and to compare symptoms between homozygous and heterozygous children. MATERIALS AND METHODS:...

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Identifiers

PMID: 29505478
DOI: 10.1097/MEG.0000000000001108

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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