The 66th Annual Meeting of the Japanese Society of Child Neurology

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General Oral Presentation

[O29] 遺伝・先天異常 1

Sat. Jun 1, 2024 8:30 AM - 9:30 AM Room8 (Bldg.1 3F 131＋132)

Organizer:Mie Inaba(Department of Pediatrics,Medical Genetics, Aichi Developmental Disability Center Central Hospital),Naoko Ishihara(Department of Pediatrics, Fujita Health University School of Medicine)

[O29-6] A case of hemiconvulsion-hemiplegia-epilepsy:HHE with CACNA1A gene mutation

○Nakano Goto, Hirokazu Takeuchi, Kenjiro Kikuchi, Rikako Takeda, Yuko Hirata, Ryuki Matsuura, Reiko Koichihara, Shinichiro Hamano (Saitama Prefectural Children's Medical Center, Saitama, Japan)

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