It is the mission of the CSNK2B Foundation to bring awareness and education to CSNK2B Neurodevelopmental Syndrome and to enrich the lives of those affected by accelerating research, treatments and by chasing a cure for CSNK2B.
Currently there is no treatment or cure for CSNK2B
Around 75-100 patients have been diagnosed with CSNK2B Neurodevelopmental Syndrome. This number is expected to increase with the use of Exome Sequencing.