Term ID: T1671

Fragile X Syndrome

/fragile-x-syndrome/
A genetic disorder caused by mutations in the FMR1 gene, resulting in intellectual disability, behavioral characteristics, and often autism spectrum features, representing a leading genetic cause of autism.
Example: Children with characteristic physical features, intellectual disabilities, social anxiety, and often autism-like behaviors including repetitive movements and difficulty with social interaction.

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Reference: Hagerman (2002)