How to Advance Prader-Willi Syndrome Research
Advancing Prader-Willi Syndrome Research: A Definitive Guide Prader-Willi Syndrome (PWS) is a complex, lifelong neurodevelopmental disorder affecting an estimated 1 in 15,000 to 20,000 live births. Characterized by a constellation of symptoms including severe hypotonia in infancy, distinctive facial features, short stature, hypogonadism, cognitive impairment, and a insatiable hunger (hyperphagia) leading to morbid obesity and … Read more