Four years on, Sarah Rowantree still questions what happened in the final weeks of her son Ryan McLaughlin’s life. The ...

Family genetics evaluations. Several family visits with the geneticist and subsequent laboratory evaluations revealed that Bobby had PWS. It was also established that his siblings did not have the ...

Juliana Steffan's mother, April Steffan, created a YouTube video about Prader-Willi syndrome, a rare genetic disorder that causes a chronic feeling of hunger, among other physical, mental and ...

Prader-Willi syndrome or PWS is a rare condition that can affect children from 0 to 6 years of age. It is a multisystem genetic disorder caused by the loss of paternally expressed genes on chromosome ...

POMONA ‒ When you fill up through October at the Mt. Ivy Country Corner's Shell gas pumps, a slice of the profits will go to helping kids like 3-year-old Catalina Valenti, who lives with Prader-Willi ...

PENNSAUKEN — A local teenager has died after a life-long battle against a rare disorder. Alexander Tran, 17, was looking forward to graduation next year from Pennsauken High School student, his family ...

VYKAT™ XR diazoxide choline treats hyperphagia in PWS in adults and children 4+. See Important Safety Info at VYKATXR.com.

(RTTNews) - Tonix Pharmaceuticals Holding Corp. (TNXP) Monday said it received clearance from the Food and Drug Administration (FDA) for the Phase 2 study of TNX-2900 to treat Prader-Willi Syndrome ...