A case of SCN8A-associated epileptic encephalopathy caused by a novel heterozygous mutation: Where is the origin of refractory startle reflex and myoclonus?

Nahoko Ueda K

[P-40] A case of SCN8A-associated epileptic encephalopathy caused by a novel heterozygous mutation: Where is the origin of refractory startle reflex and myoclonus?

Nahoko Ueda K¹, Yuichi Abe¹, Ryosuke Urabe¹, Michiko Kawai¹, Sato Suzuki-Muromoto¹, Go Takei¹, Itaru Hayakawa¹, Masaya Kubota¹, Mitsuhiro Kato² (1.Division of Neurology, National Center for Child Health and Development, Japan, 2.Department of Pediatrics, Showa University School of Medicine, Japan)

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[P-40] A case of SCN8A-associated epileptic encephalopathy caused by a novel heterozygous mutation: Where is the origin of refractory startle reflex and myoclonus?

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