Prader-Willi syndrome is a rare genetic disease that causes poor feeding in infancy but later triggers insatiable hunger.

May 15 marks National Prader-Willi Syndrome Awareness Day. For one Virginia father, the date is more than just a spot on the ...

Federal regulators are clearing a first-of-its-kind treatment for symptoms of a rare neurodevelopmental disorder that is characterized by insatiable hunger. The Food and Drug Administration approved a ...

A key feature of Prader-Willi syndrome is a constant sense of hunger that usually begins at about 2 years of age. People with Prader-Willi syndrome want to eat constantly because they never feel ...

"These medications are becoming increasingly available and should never be purchased online for people with PWS. The Prader Willi Syndrome Association UK (PWSA UK) can provide advice and ...

In Malaysia, PWS is classified as a rare disease, with a prevalence of one in every 15,000 people. According to the Prader-Willi Syndrome Association of Malaysia, 195 cases have been identified as ...

Stacy Ward, CEO of the Prader-Willi Syndrome Association, USA, believes the approval addresses “longstanding unmet needs” of people with PWS and their families. “Our families experience ...

US FDA Approves First Treatment for Rare Genetic Disorder Prader-Willi Syndrome By Sneha S K (Reuters ... which affects about 50,000 people in the U.S., impacts everyday aspects of life, such ...

Families of people with PWS have been prisoners in ... Chief Executive Officer of the Prader-Willi Syndrome Association | USA. “Our families experience the constant and disruptive challenges ...