Prader–Willi syndrome
/pɹˈeɪdɚ wˈɪli sˈɪndɹoʊm/
/pɹˈeɪdə wˈɪli sˈɪndɹəʊm/
PWSPrader–Willi syndrome
01
متلازمة برادر-ويلي, مرض برادر-ويلي
a genetic disorder with symptoms like insatiable appetite, obesity, intellectual disability, and developmental delays caused by gene deletion or loss of function on chromosome 15
