Fragile X Syndrome

What is Fragile X Syndrome?

Fragile X Syndrome is a genetic disorder caused by changes in the FMR1 gene, causing them to not create the FMRP protein that is necessary for normal brain development. Fragile X Syndrome is rare, affecting only 1 in 7,000 males and 1 in 11,000 females. Signs and symtoms include developmental delays, social and behavioral problems, and learning disabilities.