Fragile X syndrome (FXS) is an inherited genetic developmental condition that strongly impacts brain development. Despite the syndrome stemming from an altered genetic code for the single protein fragile X messenger ribonucleoprotein (FMRP), its symptoms are broad and variable; people with FXS can have a range of behavioral and physical symptoms, and around 40% of people with FXS also have autism spectrum disorder. There is currently no cure for FXS; treatments are limited to medications and therapies to help manage symptoms.
This article was originally published on MedicalXpress.com
