Prader-Willi syndrome is a genetic condition that results in a number of physical, mental, and behavioral concerns.
A key feature of Prader-Willi syndrome is a constant sense of hunger that usually begins at about two years of age.
Prader-Willi syndrome affects 350,000 people worldwide.
Resources
Prader-Willi Syndrome Association supports not only individuals diagnosed with Prader-Willi syndrome, but also their families and providers with critical information and resources.
Foundation for Prader-Willi Research works to to eliminate the challenges of Prader-Willi syndrome through the advancement of research and therapeutic development.
Bright Expectations
Find information on evaluation and intervention services, support programs for families, resources for health care providers, and information on developmental disabilities