What is Fragile X

Fragile X-associated disorders include a wide range of physical, intellectual, and behavioral symptoms that can affect family members in many different ways.

The Basics

Fragile X 101

An overview of the Fragile X disorders caused by a mutation of the FMR1 gene.

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Newly Diagnosed

Resources and advice to help navigate and understand your Fragile X diagnosis.

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Fragile X Topics

Prevalence

It is estimated that the number of individuals diagnosed with Fragile X syndrome is about 1 in 7,000 males and about 1 in 11,000 females.

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A young toddler and a clinician.

Signs & Symptoms

A look at the possible signs and symptoms of the Fragile X premutation, full mutation Fragile X syndrome, FXTAS, and FXPOI.

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A family with a dad, mom, young daughter, and an infant.

Testing & Diagnosis

Fragile X testing, analysis, and diagnosis are complicated subjects. We have extensive information for both parents and medical providers.

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Three generations of one family.

Genetics & Inheritance

Even for genetics professionals, FMR1 inheritance is complex and confusing, so it’s no surprise that families often have questions about the genetics of Fragile X.

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Treatment Recommendations

Resources and advice to help navigate and understand your Fragile X diagnosis from the experts that make up the Fragile X Clinical & Resource Consortium.

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