Angelman
Syndrome

Most people have never heard of Angelman syndrome (AS), but scientists believe that AS has the greatest potential for being cured when compared to other neurogenetic disorders.

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Newly Diagnosed

You’ve found your way to our website and a support system that will help you understand Angelman syndrome and make sense of your child’s diagnosis. Here are two things we want you to know right away:

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THERE IS HOPE FOR TREATMENT AND A CURE.

Angelman syndrome has been cured multiple ways in mice, and the progress our scientists are making is nothing short of thrilling.

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YOU ARE NOT ALONE.

We are all parents of children with Angelman syndrome, and we’re standing by to answer questions and assist you.

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Next Steps

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Understanding[clear-break]
Angelman Syndrome

Angelman syndrome (AS) is a rare neurogenetic disorder that affects approximately one in 15,000 people – about 500,000 individuals worldwide. Symptoms typically include difficulty suckling and eating, gastrointestinal issues, delayed crawling and babbling, balance and motor impairment, and seizures.

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Causes

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Testing

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Diagnosis

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Research & Impact

Our sole mission is to cure Angelman syndrome. That’s why FAST brought together a multidisciplinary team of more than two-dozen scientists from top research universities and pharmaceutical companies. These men and women are the nation’s foremost authorities on Angelman syndrome (AS), and they have joined forces on a focused path to a cure.

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