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Prevalence of Alpha-1 Antitrypsin Deficiency Alleles in a Lithuanian Cohort of Wheezing Small Children.

Advances in respiratory medicine - 5 Aug 2024

Poluzioroviene Edita, Chorostowska-Wynimko Joanna, Petraitiene Sigita, Strumila Arunas, Rozy Adriana, Zdral Aneta, Valiulis Arunas

Abstract excerpt

Severe inherited alpha-1 antitrypsin deficiency (AATD) is an autosomal genetic condition linked to chronic obstructive pulmonary disease (COPD). The significance of heterozygous, milder deficiency variants (PiSZ, PiMZ, PiMS) is less clear. We studied AATD genotypes in 145 children (up to 72 months old) with assessed wheezing severity using the Pediatric Respiratory Assessment Measure (BCCH PRAM score). A control...

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Identifiers

PMID: 39194420
DOI: 10.3390/arm92040028
PMCID: PMC11351570

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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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