CDKL5 South Asia

CDKL5 is a rare genetic disorder that primarily affects girls. It is caused by mutations in the CDKL5 gene and is characterized by early-onset seizures, developmental delay, and severe neurodevelopmental impairment. Unfortunately, there is currently no cure for this condition, and treatment options are limited.

To address this critical unmet need, we have established a CDKL5 South Asia (and working jointly with our global community CDKL5 Alliance). Our goal is to bring together patients, families, and caregivers to exchange information, share experiences, and collaborate in the search for better treatments and a cure. Also, to raise awareness of the condition amongst the medical, scientific and pharmaceutical communities, whilst ultimately supporting our children and families.