Pagnier J, Amegnizin K P, Labie D, Hayat M
Acta Haematol. 1979;61(1):27-32. doi: 10.1159/000207622.
A Basque Spanish family with heterozygous deltabeta-thalassemia is described. Patients with this anomaly usually present hematological findings observed in classical beta-thalassemia, but clinical conditions and unbalanced chain synthesis are less severe. Our propositus, however, presented clinical and biosynthetic data similar to those described in thalassemia intermedia. A family study was also performed.
