All you need to know about: Fragile X syndrome
Fragile X syndrome is a genetic condition caused by a mutation in the FMR1 gene that disrupts brain development. It is a leading inherited cause of intellectual disability and is often associated with autism spectrum disorder.
Why it matters
Understanding the genetic basis of this syndrome is essential for early diagnosis and the development of targeted support strategies for affected individuals.
Fragile X syndrome is a rare genetic condition that can affect how a child learns, speaks, behaves and develops. Caused by a mutation in a gene on the X chromosome, it is among the most common inherited causes of intellectual disability and may also be linked to autism spectrum disorder. Here is all you need to know about the condition.
The content is purely educational and based on medical consensus provided by health organizations.
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