What is the Prada-Willi syndrome?

Prader-Willi syndrome (PWS) is a genetic disorder caused by the loss of function of specific genes on chromosome 15, typically due to deletion or uniparental disomy. It is characterized by symptoms such as hypotonia, developmental delays, and an insatiable appetite leading to obesity if not managed. Individuals with PWS may also experience behavioral issues, cognitive impairment, and hormonal imbalances. Early intervention and a structured environment can help manage symptoms and improve quality of life.