how is Fragile X identified?

Fragile X can be diagnosed by a simple blood test, which can be used to identify affected [full mutation] individuals and carriers [with a pre-mutation] as well as for pre-natal diagnosis. Families should seek a referral to the National Centre for Medical Genetics, Our Lady's Hospital for Sick Children, Crumlin, Dublin 12 (01 409 6902) from their doctor or specialist.