Natural History Studies (NHS) are important in understanding the natural progression of a condition. This information can then be used to predict what may happen in the future when children are diagnosed with genetic epilepsies, and are essential when planning trials of treatment. We talk with Dr Katherine Howell, the principal investigator of the international SCN2A Natural History Study.

Hosted by Kris Pierce and David Cunnington, parents of Will, who has SCN2A.

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Links: 

• SCN2A Encephalopathy –   2015
• Genetic and phenotypic heterogeneity in SCN2A – 2017 (Marcus Wolff)
• Email to register interest in participating in natural history study

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