Prader-Willi Syndrome

Prader willi syndrome ribbon Prader-Willi syndrome is a rare genetic condition that causes learning difficulties, various physical symptoms, and behavioural challenges. The condition is caused by missing genetic material on chromosome 15. Excessive appetite and outbursts of physical aggression can present dangers for those with Prader-Willi syndrome, and it is crucial to have access to high-quality care. Without proper support and management, food-seeking behaviours can lead to life-threatening obesity. If your family cannot provide you with care, you may need a supported living arrangement or residential care. Prader-Willi Syndrome Association UK has information on securing professional support, care, and advice for living with and caring for someone with Prader-Willi syndrome.