Children with this condition develop an insatiable appetite that leads to obesity, diabetes, hypertension, and behavioral problems when not treated.

Prader-Willi syndrome is a genetic condition that can affect anyone, and manifest itself through physical symptoms, learning difficulties, and behavioral problems.

A comprehensive review published in Genomic Psychiatry synthesizes the latest understanding of Prader-Willi syndrome, revealing how this rare genetic disorder provides a unique framework for ...

People with Prader-Willi syndrome feel as if they're constantly starving. They can't be left unattended with food or they can eat themselves to death.

Prader-Willi syndrome (PWS) is a rare genetic neurodevelopmental disorder caused by an abnormality in the gene expression on chromosome 15. The Prader-Willi Syndrome Association USA estimates that ...

About PWS Prader-Willi syndrome (PWS) is a rare genetic neurodevelopmental disorder caused by an abnormality in the gene expression on chromosome 15.

About PWSPrader-Willi syndrome (PWS) is a rare genetic neurodevelopmental disorder caused by an abnormality in the gene expression on chromosome 15. The Prader-Willi Syndrome Association | USA ...

The FDA has approved diazoxide choline (VYKAT XR) as a drug to treat hyperphagia, an uncontrollable urge to eat, in people with Prader-Willi syndrome, a rare life-threatening genetic disorder.