CDKL5 syndrome Forum
- 38 members
- 10 discussions
Rare genetic disease caused by the mutation of the CDKL5 gene and characterised by early-onset drug-resistant epileptic seizures, significant neurodevelopmental impairment and severe delay in the development of motor skills
Treatments for CDKL5 Deficiency Disorder
CDKL5 Deficiency Disorder: what can you say about the treatment plan?
