As for what it’s like to live with Prader-Willi Syndrome, Meagan doesn’t hold back. “I’ll try to put it the best way I can,” she said.

Prader-Willi syndrome is a rare, complex genetic condition that affects many aspects of a person’s life and is usually apparent soon after birth. It results in physical, mental, and behavioral ...

Hyperphagia is one of the most serious and defining characteristics of Prader-Willi syndrome. Credit: Catherine Falls Commercial via Getty Images. ·Pharmaceutical Technology·Catherine Falls ...

For additional information about the conference, please see: About PWS Prader-Willi syndrome (PWS) is a rare genetic neurodevelopmental disorder caused by an abnormality in the gene expression on ...

This Prader-Willi Syndrome Awareness Day, May 15, join Soleno Therapeutics in sharing messages of hope and kindness for the Prader-Willi syndrome communityREDWOOD CITY, Calif., May 15, 2024 (GLOBE ...

Prader-Willi syndrome, which strikes only 1 in 15,000 people, can cause learning issues, muscles weakness, a slow metabolism and an insatiable appetite.

Quiver AI Summary Soleno Therapeutics, Inc. announced its participation in the 2025 United In Hope: International Prader-Willi Syndrome Conference, scheduled for June 24-28, 2025, in Phoenix, AZ.

The Prader-Willi Syndrome Association | USA estimates that PWS occurs in one in every 15,000 live births. The defining symptom of PWS is hyperphagia, a chronic and life-threatening condition ...