G08: Science Genetic Disorders: Pradder-Willi Syndrome

Prader-Willi syndrome (PWS) is a genetic multisystem disorder characterized during infancy by lethargy, diminished muscle tone (hypotonia), a weak suck and feeding difficulties with poor weight gain and growth and other hormone deficiency. In childhood, features of this disorder include short stature, small genitals and an excessive appetite.

Mission: To enhance the quality of life of and empower those affected by Prader-Willi syndrome.

PWSA UK is a small charity providing lifelong support to all those affected by Prader-Willi syndrome (PWS). We provide a dedicated helpline, a comprehensive information hub, a regional network of peer support groups with a varied programme of community events, training for professionals working with people with PWS, and support for vital research.