Скачать или смотреть All About the WSS Foundation

Hear from families with WSS warriors. Learn about their journey and the impact and importance of the WSS Foundation.

Wiedemann-Steiner Syndrome (WSS) is an extremely rare genetic disorder that affects the eleventh chromosome on the KMT2A gene. Currently, there are less than 1,000 cases known in the world. This rare disease causes a myriad of medical and developmental issues. Very little is known about WSS.

There is an ongoing therapeutic revolution for genetic disorders. However, more research is needed so that those therapies can impact WSS as soon as possible. Research is currently funded by families of children with WSS and they need your help.

To get involved visit www.wssfoundation.org.