Pediatric Neurology Briefs (Nov 2011)

Indications for Genetic Testing for Dravet Syndrome

  • J Gordon Millichap

DOI
https://doi.org/10.15844/pedneurbriefs-25-11-7
Journal volume & issue
Vol. 25, no. 11
pp. 86 – 86

Abstract

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Researchers at the Cincinnati Children’s Medical Center, OH investigated the predictive value of features of Dravet syndrome, as defined by the International League Against Epilepsy, as criteria for a positive SCN1A gene mutation in a cohort of consecutively tested children.

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