Prader Willi Syndrome

Prader Willi Syndrome
Prader-Willi syndrome is a rare genetic disease that life-threatening obesity in many children. It is a congenital (present at birth) diseases related to an abnormality of chromosome 15, which results in a series of physical, mental and behavioral disorders. This disease was found by Swiss doctors Prader A., A. Labhart and H. Willi in 1956. It is assumed that the symptoms of Prader-Willi Syndrome (PWS),