Understanding Prader-Willi Syndrome: A Comprehensive Guide
rader-Willi Syndrome (PWS) is a rare genetic disorder that impacts many aspects of a person’s life, from physical development to behavior. First identified in 1956 by Swiss doctors Andrea Prader, Alexis Labhart, and Heinrich Willi, this condition has been the focus of extensive research ever since. This guide aims to provide an in-depth understanding of Prader-Willi Syndrome, covering its symptoms, genetic basis, causes, treatments, and more. Prader-Willi Syndrome Symptoms The symptoms of Prader-Willi Syndrome can
