Research articles on fragile X syndrome

Research articles on fragile X syndrome explore how genetic changes cause this inherited condition, which affects intellectual development and behavior. Scientists study the FMR1 gene mutation responsible for the syndrome, investigating ways it impacts brain function and identifying potential treatments. These studies aim to better understand the disorder, improve diagnosis, and develop therapies to support individuals with fragile X syndrome and their families. The research often involves genetics, neuroscience, and clinical trials to find effective interventions and improve quality of life.