Genetic condition awaiting consideration - Alpha Thalassemia
Alpha Thalassemia is a severe haematological disorder resulting from mutations in the alpha globin genes. Each person has 4 alpha globin genes, if all 4 genes are mutated or deleted no alpha globin chains can be formed in a baby and the disorder will result in a hydropic baby which will either die before or at birth. It is inherited in an autosomal dominant fashion, so each embryo is at 25% risk of being affected.
Have your say on conditions awaiting consideration
If you have any feedback on the genetic conditions awaiting consideration by the HFEA, send us an email and we will discuss your comments at the next Licence Committee.
Email: pgd@hfea.gov.uk
Page last updated: 28 January 2013