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[Study of the frequency of different phenotypes of alpha-1-antitrypsin in a population of Barcelona].

Medicina clinica - 6 Jul 1996

Vidal R, Miravitlles M, Jardí R, Torrella M, Rodríguez-Frías F, Moral P, Vaqué J

Abstract excerpt

BACKGROUND: Severe alpha-1-antitrypsin (AAT) deficiency is caused by homozygous inheritance of gene Z, and is associated with a high risk of developing pulmonary emphysema. Determination of frequencies of different genes associated with the deficiency (especially S and Z) gives a clue to estimate the number of individuals homozygous PiZZ, carrying a high risk for pulmonary disease, in any given population....

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PMID: 8755448

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

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[Study of the frequency of different phenotypes of alpha-1-antitrypsin in a population of Barcelona].PMID 8755448Read ↗

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Frequency of alleles and genotypes associated with alpha-1 antitrypsin deficiency in clinical and general populations: Revelations about underdiagnosis.Semantic proximity Read ↗

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Alpha-1 antitrypsin deficiency in Italy: regional differences of the PIS and PIZ deficiency alleles.Semantic proximity Read ↗

Alpha1-antitrypsin Pi phenotypes S and Z in Spain: an analysis of the published surveys.Semantic proximity Read ↗

Frequency of Rare Alpha-1 Antitrypsin Variants in Polish Patients with Chronic Respiratory Disorders.Semantic proximity Read ↗

Alpha-1-antitrypsin PI phenotypes S and Z in Europe: an analysis of the published surveys.Semantic proximity Read ↗

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Estimated Prevalence and Number of PiMZ Genotypes of Alpha-1 Antitrypsin in Seventy-Four Countries Worldwide.Semantic proximity Read ↗

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