Prader–Willi syndrome is a rare genetic disorder in which up to seven genes on chromosome 15 are deleted or unexpressed on the paternal chromosome.
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Sites 11
- Prader-Willi Alliance of New York Represents the interests of individuals in New York State with Prader-Willi syndrome, their families, and the professionals who provide services to the Prader-Willi population.
- Prader-Willi Syndrome Association (USA) Characteristics include hypotonia, insatiable appetite, obesity if food intake is uncontrolled, hypogonadism and incomplete sexual development, developmental delays, variable degrees of mental retardation or functional retardation, short stature (adult), small hands and feet, mild dysmorphology, and behavior problems which can be severe.
- The Foundation for Prader-Willi Research A non-profit group of volunteer families, friends and researchers aiming to raise funds for research into finding treatments.
- Latham Centers A residential facility, located on Cape Cod, USA, for the treatment of adults and children with Prader-Willi Syndrome. Includes details about diet, medical news, the programs, and consulting services.
- The Prader-Willi Syndrome Association (UK) Charitable organization providing support to people with PWS, their families and carers, and the professionals who work with them. Includes information and resources.
- Gretton Homes Information about the organization that offers residential care in the UK for people with Prader-Willi syndrome.
- Foundation for Prader Willi Research Canada Charitable organization dedicated to eliminating Prader-Willi Syndrome through the advancement of research. Includes information, details of research projects and how members of the public can get involved.
- Patient UK: Prader-Willi Syndrome Provides information for medical professionals on this complex genetic disorder.
- University of Michigan Health System: Prader-Willi Syndrome Information about this syndrome in children and links to relevant articles and organizations providing advocacy and support.
- Prader-Willi and not feasting at Christmas The BBC reports on a 16-year-old with a condition that means she never feels full, and the meticulous meal planning that goes into Christmas.
- GeneReviews: Prader-Willi Syndrome Summary, diagnosis, clinical description, differential diagnosis, management, genetic counseling and molecular genetics.