It was then tested on 16,579 newborns in Victoria with the test identifying two with Prader Willi, two with Angelman and one with Dup15q. The three rare disorders are characterised by varying degrees ...

Prader Willi Syndrome: The girl who never feels full By Peter Meiszner Global News Posted August 11, 2013 8:21 pm Updated August 11, 2013 10:59 pm ...

Per the PWS Association USA, approximately one in every 15,000 newborns suffers from this rare genetic disorder. The most common symptom of PWS is hyperphagia, an abnormally increased appetite for ...