Prader-Willi syndrome is a genetic condition that can affect anyone, and manifest itself through physical symptoms, learning difficulties, and behavioral problems.

New approach finds ‘parent-of-origin’ effects in more than a dozen genes — without the need for parental data.

Prader-Willi and Angelman syndromes are rare genetic disorders affecting about 1 in 10,000 to 30,000 and 1 in 12,000 to 20,000 people around the world, respectfully.

The Prader–Willi syndrome market is experiencing growth due to increasing in diagnosis rate owing to an increase in genetic testing, more and more identification of other lesser-known genetic ...

DelveInsight’s "Prader–Willi Syndrome Market Insights, Epidemiology, and Market Forecast – 2034" report delivers an in-depth understanding of PWS, historical and forecasted epidemiology as ...

Prader Willi Syndrome: The girl who never feels full By Peter Meiszner Global News Posted August 11, 2013 8:21 pm Updated August 11, 2013 10:59 pm ...

Angelman syndrome shares symptoms and characteristics with other disorders like autism, cerebral palsy and Prader-Willi syndrome, which is why 50% of individuals are originally misdiagnosed, according ...

People enrolled in the study were 4 years old or older with Prader-Willi syndrome and excessive hunger and had already been taking Vykart XR for an average of 3.3 years (range: 2.5 to 4.5 years).

Management of Prader-Willi Syndrome: A book edited by Merlin Butler, Phillip D.K. Lee, and Barbara Y. Whitman, that is endorsed by the Prader-Willi Syndrome Association as a comprehensive resources.