Alfa1-antitripszin fenotípusok gyakorisága Magyarországon.

Translated title of the contribution: Prevalence of the alpha-1 antitrypsin phenotype in Hungary

László Szónyi, Mariann Dobos, Barna Vásárhelyi, Erika Héninger, Zsuzsa Váczi

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INTRODUCTION: Alpha-1-antitrypsin deficiency is one of the most common inherited metabolic disorders. The presence of PiZ and PiS alleles alpha-1-antitrypsin deficeing are associated with. The geographical distribution of PiZ and PiS is heterogenous in Europe. AIM: The aim of the study was to investigate the frequency of alpha-1-antitrypsin alleles with isoelectric focusing in 789 healthy Hungarian citizens and to compare the results to those obtained in other European countries. The measurements were done in the Laboratory of the Institute of Experts in Forensic Medicine. RESULTS: The frequency of PiM, PiZ and PiS alleles were 97.2%, 0.95% and 1.65% respectively. Therefore, the hypothetical prevalences of PiZZ and PiSS alleles are 1:10526 and 1:6060, respectively. CONCLUSION: These results do not differ significantly from those found in the neighbouring countries. Further investigation is needed to elucidate the possible role of alpha-1-antitrypsin phenotypes in the pathogenesis of chronic liver disorders and lung emphysema.

Translated title of the contributionPrevalence of the alpha-1 antitrypsin phenotype in Hungary
Original languageHungarian
Pages (from-to)705-708
Number of pages4
JournalOrvosi hetilap
Issue number15
Publication statusPublished - Apr 13 2003

ASJC Scopus subject areas

  • Medicine(all)

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    Szónyi, L., Dobos, M., Vásárhelyi, B., Héninger, E., & Váczi, Z. (2003). Alfa1-antitripszin fenotípusok gyakorisága Magyarországon. Orvosi hetilap, 144(15), 705-708.