Stem cell researchers have reversed Prader-Willi syndrome in brain cells growing in the lab. The discovery provides clues that could lead to a treatment for Prader-Willi, a genetic disorder that ...

Prader-Willi syndrome is a genetic disorder caused by changes to chromosome 15. It affects growth, behavior, and learning and requires continual management to avoid potentially life threatening ...

An Australian study reveals that people with the rare genetic disorder known as Prader-Willi Syndrome may have an impaired autonomic nervous system. This discovery opens up a new way of looking at the ...

Andrea Prader and Heinrich Willi, two Swiss pediatricians, and Alexis Labhart, an internist, first described Prader-Labhart-Willi Syndrome in 1956. Prader was an influential figure in European ...

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 ...

Haley Kavrell, 17, who must cope with Prader-Willi syndrome, which causes her to feel constant hunger, picks basil at her home in Davis late last month. Renée C. Byer [email protected] After receiving ...

This story was originally published on BioPharma Dive. To receive daily news and insights, subscribe to our free daily BioPharma Dive newsletter. Acadia Pharmaceuticals is giving up on a drug to treat ...

For now, all Jenny Welch can do is wait. Every day and often long into the night, the 27-year-old single mom from Montague keeps vigil at the bedside of her critically ill infant daughter, EllyAnnah, ...