Placebo group: The other group took dummy pills (placebo). Both groups also went on a high-fiber, low calorie diet. These were the results of the 12 week study, which was published in The Journal of The American Medical Association (a highly respected scientific journal): Heymsfield, et al. 1998 As you can see, both groups lost weight.
Clinical Trials investigating potential treatments for Prader-Willi syndrome are taking place around the country! FPWR is dedicated to sharing information on study opportunities and how you can participate.
Prader-Willi syndrome is a large window of opportunity for researchers. PWS was one of the first genetic models to reveal the importance of imprinting and has provided other breakthrough insights in .
Prader-Willi Research Foundation of Australia The Prader-Willi Research Foundation of Australia works to improve clinical outcomes and treatments for Prader-Willi syndrome. By focusing on both short and long term outcomes, our research program will change . Intellectual and developmental disabilities (IDDs), including Prader-Willi syndrome, are a primary focus of the NICHD’s research. Prader-Willi syndrome encompasses a set of related conditions with a range of symptoms that affect eating and metabolism, growth, behavior, and intellectual development.
Jul 07, · Prader-Willi syndrome (PWS) is a genetic condition that affects many parts of the body. Infants with PWS have severe hypotonia (low muscle tone), feeding difficulties, and slow growth. In later infancy or early childhood, affected children typically begin to eat excessively and become obese. Prader-Willi California Foundation looks for every opportunity to support PWS research and we encourage families to participate in PWS research studies as well. Explore the pages in this section to find research opportunities for your family, read results from past studies, find research conferences to attend, or learn about how to obtain a grant to present your research at a conference.