
Prader–Willi Syndrome: Understanding the Genetic Disorder Affecting Children
Prader–Willi Syndrome (PWS) is a complex genetic disorder that manifests with a variety of physical, behavioral, and cognitive challenges. Typically identified in early childhood, PWS is characterized by hypotonia (poor muscle tone), feeding difficulties, and developmental delays. As children grow, they often exhibit hyperphagia (an insatiable appetite) leading to obesity if not carefully managed. Distinctive…