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alpha-Thalassaemia and hyperbilirubinaemia in G-6-PD-deficient newborns.
  1. T Meloni,
  2. R Corti,
  3. S Costa,
  4. G Mele,
  5. V Franca

    Abstract

    53 newborn infants with both G-6-PD deficiency (29 male hemizygotes and 24 female heterozygotes) and alpha-thalassaemia, and 120 newborn infants with only the enzymatic defect (60 male hemizygotes and 60 female heterozygotes) were studied. 12 of those with both G-6-PD deficiency and alpha=thalassaemia, and 32 of those with only G-6-PD deficiency showed hyperbilirubinaemia. alpha-Thalassaemia does not seem to be implicated in the development of hyperbilirubinaemia in G-6-PD-deficient newborns.

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