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About fragile x syndrome key points fragile x syndrome (fxs) is a genetic disorder and one of the most common causes of inherited intellectual disability Explore symptoms, inheritance, genetics of this condition. Fxs affects both males and females

However, females often have milder symptoms than males. Fragile x syndrome is a genetic condition that causes a range of developmental problems including learning disabilities and cognitive impairment Fragile x syndrome (fxs) fragile x syndrome is the leading cause of inherited intellectual disabilities

There are behavioral, physical, intellectual and mental health symptoms

Although there isn’t a cure, medication and therapy can help manage symptoms. Fragile x syndrome tends to show more symptoms on affected males since females have another x chromosome which can compensate for the damaged one [4][11] fragile x syndrome is the most common cause of inherited intellectual disability, affecting an estimated 1 per 4,000 people It is also the most common single gene cause of autism

Fragile x syndrome (fxs) is a genetic condition that can cause learning, behavior, and developmental challenges, as well as various physical characteristics It is the most common inherited cause of intellectual disability and is the leading known genetic cause of autism Fxs occurs when a change in the fmr1 gene on the x chromosome affects how the brain develops and functions Fragile x syndrome is a condition that affects a child's learning, behavior, appearance, and health

Learn more about symptoms, causes, and treatment at webmd.

The genetic disorder fragile x syndrome, which results from mutations in a gene on the x chromosome, is the most commonly inherited form of developmental and intellectual disability. Fragile x syndrome is an inherited intellectual disability caused by a mutation in the fmr1 gene.

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