Beck-Fahrner Syndrome Foundation

Our mission is to accelerate full spectrum research to cure Beck-Fahrner syndrome (TET3 deficiency) and to empower affected families with information, knowledge, and connectivity. Our organization supports this mission by prioritizing and focusing on efforts that:

Increase awareness and understanding of Beck-Fahrner syndrome
Advance access to a Beck-Fahrner syndrome diagnosis
Empower, connect, and support affected families
Establish partnerships among medical, scientific, and patient communities
Accelerate full spectrum research to develop a cure for Beck-Fahrner syndrome