Prader-Willi Syndrome

A comprehensive, multidisciplinary clinic serving patients with Prader-Willi syndrome recently opened at Monroe Carell Jr. Children’s Hospital at Vanderbilt. Prader-Willi syndrome (PWS) is a complex genetic disorder that affects appetite, growth, metabolism, cognitive function and behavior. It is characterized by the inability to achieve satiety, developmental delays and intellectual disability,… Read More

A mutation associated with epilepsy and autism also is responsible for a “pale eye” trait in two rare genetic disorders, Angelman syndrome and Prader-Willi syndrome, neuroscientists at Vanderbilt University Medical Center reported this week. Read More

Children with Prader-Willi Syndrome who received growth hormone treatment had cognitive advantages compared to untreated patients. Read More