Fragile X syndrome is a genetic condition that causes a range of developmental problems including learning disabilities and cognitive impairment. Explore symptoms, inheritance, genetics of this condition.| medlineplus.gov
Fragile X-associated tremor/ataxia syndrome (FXTAS) is characterized by problems with movement and thinking ability (cognition). Explore symptoms, inheritance, genetics of this condition.| medlineplus.gov
Fragile X-associated primary ovarian insufficiency (FXPOI) is a condition that affects women and is characterized by reduced function of the ovaries. Explore symptoms, inheritance, genetics of this condition.| medlineplus.gov
Due to the variability of its symptoms, a conclusive diagnosis of fragile X syndrome can only be obtained with genetic testing.| Fragile X News Today
Read about the characteristic symptoms of fragile X syndrome, which range from developmental and behavioral problems to physical features.| Fragile X News Today
Fragile X syndrome is caused by low to no levels of the FMRP protein, important for brain development, due to mutations in the FMR1 gene.| Fragile X News Today
