🔬 Today on #FragileXAwarenessDay, we reaffirm our commitment to advancing research in rare neurological disorders.
Fragile X syndrome, caused by a change in the FMR1 gene, is one of the leading known genetic causes of autism spectrum disorder and affects ~1 in 7,000 males and 1 in 11,000 females.
At Servier, we aim to become a global leader in rare neuro diseases by 2030 and strengthened this ambition in 2025 with the acquisition of a potential Fragile X treatment. 
Learn more about Fragile X syndrome 🔗 https://f.mtr.cool/vpnyhtw9qr
#WeAreServier #MovedByYou #RareDiseases #Neurology #FragileXSyndrome