Search results
Results from the WOW.Com Content Network
The Angelman Syndrome Foundation exists to help those with Angelman syndrome and their caregivers live better lives through Research, Clinical Care, Family Support and Educational Resources. Our work is dependent on support from the Angelman community and YOU.
Angelman syndrome (AS) is a rare neuro-genetic disorder that occurs in one in 15,000 live births or 500,000 people worldwide. It is caused by a loss of function of the UBE3A gene in the 15th chromosome derived from the mother.
The mission of the Angelman Syndrome Foundation is to advance the awareness and treatment of Angelman syndrome through education and information, research, and support for individuals with Angelman syndrome, their families and other concerned parties.
The mission of the Angelman Syndrome Foundation is to advance the awareness and treatment of Angelman syndrome through education and information, research, and support for individuals with Angelman syndrome, their families and other concerned parties.
The mission of the Angelman Syndrome Foundation is to advance the awareness and treatment of Angelman syndrome through education and information, research, and support for individuals with Angelman syndrome, their families and other concerned parties.
Symptoms of Angelman syndrome. Some symptoms can vary and be more severe than others, but in most children diagnosed with AS, the following are present: Developmental delays. These can vary from individual to individual , but common delays are:
We connect those who practice evidence-based medicine for Angelman syndrome with a high level of excellence and ensure as many families have access to it as possible. ASF Clinics are part of the LADDER Learning Network.
The good news is that you found the ASF! The ASF has been supporting families for over 30 years while funding the research that has made the biggest strides toward a cure for Angelman syndrome. We and our network of families are here for you. Start with the steps below.
Genetics of AS. Angelman syndrome is caused by a problem with the UBE3A gene located at the 15th chromosome. It’s important to keep in mind that in typical humans, the UBE3A gene from our father is silent and the brain uses the UBE3A gene from our mother during development.
The mission of the Angelman Syndrome Foundation is to advance the awareness and treatment of Angelman syndrome through education and information, research, and support for individuals with Angelman syndrome, their families and other concerned parties. We exist to give all of them a reason to smile, with the ultimate goal of finding a cure.