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  • Title: Haemoglobin O Arab, beta-thalassaemia and glucose-6-phosphate dehydrogenase deficiency in a Hungarian family.
    Author: Horányi M, Szelényi J, Rona G, Lang A, Lehmann H, Hollán SR.
    Journal: Folia Haematol Int Mag Klin Morphol Blutforsch; 1980; 107(4):654-60. PubMed ID: 6162733.
    Abstract:
    A 29-year-old Hungarian woman was found to be double heterozygote for Hb O Arab and beta-thalassaemia. Haemolytic anaemia became manifest during her second pregnancy. In the course of genetic studies G-6-PD deficiency was also detected in the family. The patient originates from a North-Eastern part of Hungary which had been hydrogeologically isolated during past centuries.
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