Nov 14, 2024 · Prader-Willi (PRAH-dur VIL-e) syndrome is a rare genetic condition that leads to physical, mental and behavioral problems. A key feature of Prader-Willi syndrome is a sense …

Prader-Willi syndrome (PWS) is a rare genetic condition that affects your child’s metabolism and causes changes to their body and behavior. They have severe low muscle tone and poor …

Prader–Willi syndrome (PWS) is a rare genetic disorder caused by a loss of function of specific genes on chromosome 15. [2] In babies, symptoms include weak muscles, poor feeding, and …

Learn about Prader-Willi Syndrome, its symptoms, causes, and key facts about this rare genetic disorder. Understand treatment options.

May 30, 2012 · After infancy, symptoms of PWS include uncontrolled eating and delays in reaching physical activity milestones, such as standing and walking.

Jul 12, 2023 · Behavioral problems are common and can include temper tantrums, obsessive/compulsive behavior and skin picking. Motor milestones and language development …

Apr 28, 2025 · In early childhood, kids with PWS start to show other signs. It affects a part of their brain called the hypothalamus -- this is what tells you you're full when you eat enough food. …

Symptoms of Prader-Willi Syndrome Many symptoms of Prader-Willi syndrome vary according to the child's age. Newborns with the syndrome feel limp, feed poorly, and gain weight slowly. …

People with Prader-Willi syndrome do not usually vomit or complain about stomach pain, so take these symptoms very seriously if they happen. Call your care team or GP immediately for …

People with Prader-Willi syndrome typically have mild to moderate intellectual impairment and learning disabilities. Behavioral problems are common, including temper outbursts, …