Haemoglobin synthesis in bone marrow of patients with beta O and beta +-thalassaemia

Acta Haematol. 1981;65(3):170-6. doi: 10.1159/000207174.

Abstract

Haemoglobin synthesis was studied in bone marrow erythroblasts and in reticulocytes of 4 children with beta O-thalassaemia major and of 7 children with beta +-thalassaemia major. In patients with beta O-thalassaemia the gamma/a ratio was found to be lower in bone marrow than in peripheral blood. On the contrary, in patients with beta + thalassaemia the beta + gamma/a ratio was more balanced in bone marrow, where the beta-chain synthesis was higher, than in reticulocytes. This last result could be explained by the presence of an abnormal m-RNA for beta-chains in beta +-thalassaemia.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bone Marrow / metabolism*
  • Bone Marrow Cells
  • Child
  • Child, Preschool
  • Erythroblasts / metabolism*
  • Erythrocytes / metabolism*
  • Hemoglobins / biosynthesis*
  • Humans
  • Infant
  • Reticulocytes / metabolism
  • Thalassemia / blood
  • Thalassemia / classification
  • Thalassemia / metabolism*

Substances

  • Hemoglobins