Prader Willi Syndrome Resources

Prader-Willi Syndrome (PWS) also known as Prader-Willi Labhart Syndrome is a genetic disorder, characteristics include developmental and intellectual developmental disability, poor muscle tone, and lack of eye coordination. A complex genetic disorder impacts appetite, growth, cognitive function and behavior.


Medical Sites

Genetics Home Reference
Mayo Clinic
Medical Home Portal



Foundation for Prader-Willi Research
International Prader-Willi Syndrome Organization
Prader-Willi Syndrome Association


Management of Prader-Willi Syndrome
 Our Way of Life
Prader-Willi Syndrome: Selected Research and Management Issues



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