Angelman Syndrome Foundation
Individual & Family Services, 75 Executive Dr Ste 327, Aurora, Illinois, 60504, United States, 1-10 Employees
Phone Number: 80********
Who is ANGELMAN SYNDROME FOUNDATION
Angelman syndrome (AS) is a rare neuro-genetic disorder that occurs in one in 15,000 live births. AS is often misdiagnosed as cerebral palsy or autism due to lack of awareness. Characteri...
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Headquarters: 75 Executive Dr Ste 327, Aurora, Illinois, 60504, United States
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Employees: 1-10
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Revenue: $5 Million to $10 Million
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CEO:
Amanda Moore
Email
Phone
Industry: Individual & Family Services
SIC Code: 8322
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Frequently Asked Questions Regarding Angelman Syndrome Foundation
Answer: Angelman Syndrome Foundation's headquarters are located at 75 Executive Dr Ste 327, Aurora, Illinois, 60504, United States
Answer: Angelman Syndrome Foundation's phone number is 80********
Answer: Angelman Syndrome Foundation's official website is https://angelman.org
Answer: Angelman Syndrome Foundation's revenue is $5 Million to $10 Million
Answer: Angelman Syndrome Foundation's SIC: 8322
Answer: Angelman Syndrome Foundation has 1-10 employees
Answer: Angelman Syndrome Foundation is in Individual & Family Services
Answer: Angelman Syndrome Foundation contact info: Phone number: 80******** Website: https://angelman.org
Answer: Angelman syndrome (AS) is a rare neuro-genetic disorder that occurs in one in 15,000 live births. AS is often misdiagnosed as cerebral palsy or autism due to lack of awareness. Characteristics of the disorder include developmental delay, lack of speech, seizures, and walking and balance disorders. Individuals with Angelman syndrome will require life-long care. Because of its genetic relationship to autism and other disorders, many researchers believe that curing Angelman syndrome will lead to cures for similar disorders. Angelman syndrome research is on the cusp of potential treatments to reverse the debilitating symptoms of Angelman syndrome. The Angelman Syndrome Foundation raises funds for Angelman syndrome research and supports families. Use this website to keep abreast of current information regarding research, education, general information and therapies for Angelman syndrome. If you have any questions or would like additional information please email the ASF at info@angelman.org.
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