Additional Resources

As we learn more about CDKL5, we find that there is an array of ways that this gene mutation presents itself. Some features are closely linked with other neurological disorders, such as Rett Syndrome (RTT), Infantile Spasms(ISSX), West Syndrome, Lennox-Gastaut (LGS), Early onset Epilepsy of Infancy, and Autism.

Below are links to other rare disease organizations that have aspects associated with CDKL5.

Rare Disease Networks and Genetic Support

 

Epilepsy, Infantile Spasms, West Syndrome

 

Rett Syndrome and Rett Related Disorders

 

Autism

 

Lennox-Gastaut Syndrome (LGS)

 

See more related organizations at:  CDKL5 Organizations Around the World