A new blood test is being developed by researchers in Cambridge and Oxford, which, for the first time, could help identify babies at risk of a severe form of sickle cell disease, allowing immediate and more intensive treatment to be given, thanks to a grant from children’s charity Action Medical Research.
Over 12,000 people in the UK have sickle cell disease – the UK’s most common severe genetic disorder. An estimated 20 million people are affected worldwide.1-3 Symptoms usually start early – in babies who are just six to nine months old.