Angelman Syndrome (Subscribe)
Links
Angelman e.V.
Offizielle Seiten des deutschen Angelman-Eltern-Vereins.
Angelman Syndrome Association Australia
http://www.angelmansyndrome.org/
Angelman Syndrome (AS) is a rare neuro-genetic disorder. named after an English paediatrician, Dr Harry Angelman, who first described the syndrome in 1965.
Angelman Syndrome Foundation
The Angelman Syndrome Foundation is a national organization of families, caregivers and professionals who care about those with Angelman Syndrome. It is a member organization of the International Angelman Syndrome Organization (IASO).
As described in our by-laws, ASF's Mission 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.
Angelman Syndrome (AS) has confused the medical community and parents of Angelman children for hundreds of years. Initially presumed to be rare, it is now believed thousands of Angelman Syndrome cases have gone undiagnosed or misdiagnosed as cerebral palsy, autism or other childhood disorders. What is Angelman Syndrome? Click on the "About AS" tab to the left, and browse through our site for more information for families and professionals who want to know more about AS.
Angelman Syndrome (AS) has confused the medical community and parents of Angelman children for hundreds of years. Initially presumed to be rare, it is now believed thousands of Angelman Syndrome cases have gone undiagnosed or misdiagnosed as cerebral palsy, autism or other childhood disorders. What is Angelman Syndrome? Click on the "About AS" tab to the left, and browse through our site for more information for families and professionals who want to know more about AS.


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