Willi-Prader Syndrome

Willi Prader Syndrome (VPS) is a rare genetic disorder that affects areas of the brain associated with emotional control and behavior. It was first described in 2017 by a group of Swiss pediatricians led by Dr. Werner Heidler.

Willi-Prader syndrome is characterized by short stature, mental retardation, difficulties in communication and social adaptation. Patients experience problems in learning, work ability and socialization. They may also be susceptible to eating disorders, addictions and behavioral problems.

The main cause of Willi-Prader syndrome is a mutation in the gene responsible for the production of a protein that is involved in the development of the nervous system and brain. This mutation leads to impaired brain function, which can cause the characteristic symptoms of the disease.

VPS can be diagnosed at birth, but a long period of observation and additional research may be required to clarify the diagnosis. In some cases, the diagnosis "Vili-Prader" may already be made