Prognostic, clinical and demographic features in SCN1A mutation-positive Dravet syndrome.

@article{Brunklaus2012PrognosticCA,
  title={Prognostic, clinical and demographic features in SCN1A mutation-positive Dravet syndrome.},
  author={Andreas Brunklaus and Rachael Ellis and Eleanor Reavey and Glen Forbes and Sameer M Zuberi},
  journal={Brain : a journal of neurology},
  year={2012},
  volume={135 Pt 8},
  pages={
          2329-36
        }
}
Dravet syndrome is a severe infantile onset epileptic encephalopathy associated with mutations in the sodium channel alpha 1 subunit gene SCN1A. To date no large studies have systematically examined the prognostic, clinical and demographic features of the disease. We prospectively collected data on a UK cohort of individuals with Dravet syndrome during a 5-year study period and analysed demographic information based on UK population and birth figures. From structured referral data we examined a… CONTINUE READING

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