GPs have been urged to test patients for a genetic condition that is the most common inherited cause of learning disability. There is a “surprising lack of awareness” around Fragile X, experts said. About one in 250 women and one in 600 men are carriers of the abnormal gene that causes Fragile X, with female carriers at a higher risk of early menopause.
The syndrome is caused by an alteration to a gene on the X chromosome, which disrupts the production of a protein needed for brain development. Women with the gene have a 50% chance of passing on the condition to their children, while an affected man will pass the condition on to daughters, but not sons. Fragile X syndrome affects about one in 4,000 males and one in 6,000 females, causing a range of developmental issues.
Pete Richardson, managing director of the Fragile X Society, said: “As the most common inherited cause of learning disability, there is a surprising lack of awareness around Fragile X syndrome. “Carriers of the Fragile X pre-mutation often won’t know they are affected.” People are more likely to be carriers if they have a family history of Fragile X syndrome – or of intellectual disability, developmental delay or autism of unknown cause – as well as infertility problems associated with elevated follicle-stimulating hormone levels or premature ovarian failure.
Women with ovarian insufficiency also have a 2-15% chance of being a Fragile X carrier. Mr Richardson added: “When a woman shows signs .
