[O23] 一般演題(口演)23 てんかん：その他① | The 67th Annual Meeting of the Japanese Society of Child Neurology

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General Oral Presentation

[O23]一般演題(口演)23 てんかん：その他①

Fri. Jun 6, 2025 6:45 PM - 7:35 PM JST
Fri. Jun 6, 2025 9:45 AM - 10:35 AM UTC

第5会場

座長：赤坂紀幸(新潟県はまぐみ小児療育センター小児科),森健治(徳島大学大学院医歯薬学研究部子どもの保健・看護学分野)

[O23-01]Adult clinicians' views on transition for childhood-onset epilepsy

^○Kenjiro Kikuchi^1,2, Shin-ichiro Hamano^1,2, Azusa Oba^1,2,3, Haruhito Horita^1,2, Hirokazu Takeuchi^1,2,3, Yuko Hirata^1,2, Ryuki Matsuura^1,2,3, Reiko Koichihara^1,2, Akira Oka¹ (1.Division of Neurology, Pediatric Epilepsy Center, Saitama Children's Medical Center, Saitama, Japan, 2.Division of Neurology, Pediatric Epilepsy Center, Saitama Children's Medical Center, Saitama, Japan, 3.Department of Pediatrics, Jikei University School of Medicine, Tokyo, Japan)

[O23-02]Developmental rate is accelerated within the first year after total corpus callosotomy in children.

^○Nanako Nishiguchi¹, Ryoko Honda¹, Tomonori Ono², Noriko Ikeda¹, Tadateru Yasu¹, Hiroshi Baba³ (1.Department of Pediatrics, National Nagasaki Medical Center, Nagasaki, Japan, 2.Department of Neurosurgely, National Nagasaki Medical Center, Nagasaki, Japan, 3.Epilepsy Center, Nishi-Isahaya Hospital, Nagasaki, Japan)

[O23-03]Risk factor of epilepsy in institutionalized adult patients with severe motor and intellectual disabilities

^○Yuri Sakaguchi^1,2,3, Hideko Nakajima², Yukiko Harada², Sachi Kiguchi², Yuji Iwasaki², Asuka Sudo³, Masako Tobita³, Goro Tsuruta³, Yasuo Hachiya³, Hiromi Seki³, Tomoki Kosho¹ (1.Department of Medical Genetics, Shinshu University, Matsumoto, Nagano, Japan, 2.Department of Pediatrics, Inariyama Medical Welfare Center, Chikuma, Nagano, Japan, 3.National Hospital Organization Higashinagano Hospital, Nagano, Nagano, Japan)

[O23-04]Infantile epileptic spasms syndrome over the past 21 years at the Department of Pediatrics, Ehime University Hospital

^○Toshihiro Jogamoto, Chisato Yajima, Takahiro Motoki, Mariko Eguchi (Department of Pediatrics, Ehime University Graduate School of Medicine, Ehime, Japan)

[O23-05]A case of Dravet syndrome with ATP1A1 gene mutation in which seizures were alleviated by carnitine supplementation

^○Atsuko Oba^1,2, Hikari Oikawa^1,2, Fuyuki Miya³, Mituhiro Kato⁴ (1.Department of Pediatrics, The Jikei University Kashiwa Hospital,Chiba,Japan, 2.Department of Pediatrics, The Jikei University,Tokyo, Japan, 3.Center for Medical Genetics, Keio University School of Medicine, Tokyo, Japan, 4.Department of Pediatrics, Showa University School of Medicine,Tokyo, Japan)

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