Examination of the genetic mechanisms underlying the thalassaemias has led
to a clearer understanding of the control of eukaryotic genes in general.
Inherited disorders of haemoglobin synthesis are an important cause worldwi
de of morbidity and mortality, and place a large burden on patients, famili
es, and ultimately communities.
The haemoglobin disorders can be controlled, by counselling and prenatal di
agnosis.
Treatment is usually symptomatic, though bone-marrow transplantation for be
ta-thalassaemia may be successful in suitable patients.