The thalassaemias are a group of conditions, all of which are characterized by reduced synthesis of either the alpha (alpha-thalassaemia) or the beta (beta-thalassaemia) chain of the hemoglobin molecule.
Treatment requires repeated blood transfusions; these help to maintain normal growth and development. Without treatment, affected children fail to thrive and have a shortened life expectancy.
Beta-thalassaemia is an autosomal recessive condition caused by mutations in the beta-globin gene. The condition is extremely variable and symptoms often correlate to the specific mutations in an affected individual.
Beta-thalassaemia is common in people from the Mediterranean, the Middle East, South East Asia and the Indian sub-continent.
Individuals with beta-thalassaemia are healthy at birth, but develop a severe anemia between three months and one year of age. With modern treatment, children born in the UK with beta-thalassaemia should expect to live a near normal life expectancy.
Clinical manifestations are extremely variable.
The diagnosis depends on measuring red blood cell indices that reveal a microcytic hypochromic anaemia. Subsequent investigations should include: a peripheral blood film that shows an excess of primitive nucleated red blood cells; and hemoglobin electrophoresis that demonstrates decreased amounts of HbA and increased amounts of fetal hemoglobin (HbF) after 12 months of age.
DNA testing may be useful for predicting the clinical phenotype in some cases.
Beta-thalassaemia is an autosomal recessive condition, which means that the affected individual has two altered copies of the beta-globin gene. Each parent has one altered copy and one usual copy of the gene and are said to have beta-thalassaemia trait. They usually have mild anaemia.
Each child has a 25%, or 1 in 4, chance of inheriting the gene alteration from both parents, thus having beta-thalassemia, with the potential to develop complications of the condition.
To date, more than 200 thalassaemia disease-causing mutations have been identified in the beta-globin gene. However, four to ten mutations account for the majority of cases in the population groups where beta-thalassaemia is most common.
Management of Beta-thalassaemia
The diagnosis may be anticipated by identifying parents as carriers during antenatal screening and confirmed by prenatal diagnosis when requested, or by neonatal testing. The family can then be seen before the development of symptoms and arrangements for care discussed.
All patients should receive an optimal level of care delivered close to home as well as access to clinical experts in specialist centres.
Regular transfusions correct the anemia, but transfusional iron overload needs to be prevented by adequate iron chelation. Transfusions are usually required every three to four weeks. A definitive cure is possible following bone marrow transplantation.
Genetic testing can be used to:
identify the gene alterations in the beta-globin genes in someone with beta-thalassaemia;
provide information about the genetic status of relatives of someone with beta-thalassaemia through carrier testing; and
offer prenatal genetic diagnosis.