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Our Mission
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.
Resources
Articles related to CSNK2B
Scientific Reports
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Resources for Parents
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Report from HGVS
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POBINDS Info
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