Fragile X syndrome is a genetic condition that causes a range of developmental problems including learning disabilities and cognitive impairment.
Affected individuals usually have delayed development of speech and language by age two.Â
About one-third of individuals with fragile X syndrome have features of autism spectrum disorders that affect communication and social interaction.
Seizures occur in about 15% of males and about 5% of females with fragile X syndrome.
Bright Expectations
Find information on evaluation and intervention services, support programs for families, resources for health care providers, and information on developmental disabilities
Resources
National Fragile X Foundation works to increase public and professional awareness of fragile X to support legislative advocacy, and increase funding for research.
FRAXA Research Foundation is dedicated to finding a cure for fragile X syndrome through the funding of continued research of this condition.
National Organization for Rare Disorders is a patient advocacy organization dedicated to providing information on resources and organizations serving individuals with rare conditions.