PWS is a complex genetic disorder presenting with a spectrum of symptoms found listed throughout this website. Individuals may present with less or more of these symptoms, each in varying degrees. The typically occurring symptoms which characterise PWS can be found in ‘What is PWS?‘ below. Further information about symptoms of PWS can be found in the Medical A-Z and Support and Management sections of our website...
Prader-Willi Syndrome (PWS) is a rare and complex neurodevelopmental disorder occurring in 1 in 16,000 births, affecting approx 200 New Zealanders...
PWSA(NZ) Incorporated is a registered charity (No. CC46009). We provide advice, advocacy, information and support.
Registration numbers: CC46009 (W)