The 60th Annual Meeting of the Japanese Society of Child Neurology

Presentation information

Print

Oral Presentation

Epilepsy/Convulsion Diagnosis/Gene

[O20] Epilepsy/Convulsion Diagnosis/Gene

Fri. Jun 1, 2018 1:30 PM - 2:30 PM Room 7 (3F 304)

Chair:JUN TOHYAMA(Department of Pediatrics, Nishi-Niigata Chuo National Hospital, Niigata, Japan), Yasunari Sakai(Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University)

[O-108] Two Japanese cases of epileptic encephalopathy with FGF12 mutation

Ryo Takeguchi1, TAKEHIKO INUI2, KAZUHIRO HAGINOYA2, MICHIAKI NAGURA3, ERI TAKESHITA1, TAKASHI SAITO1, EIJI NAKAGAWA1, KENJI SUGAI1, MASAYUKI SASAKI1, YURI UCHIYAMA4, ATSUSHI FUJITA4, MITSUKO NAKASHIMA4, HIROTOMO SAITSU4, NAOMICHI MATSUMOTO4 (1.Department of Child Neurology, National Center Hospital, National Center of Neurology and Psychiatry, Tokyo, Japan, 2.Department of Neurology, Miyagi Children's Hospital, Miyagi, Japan, 3.Department of Pediatrics, Saitama Medical Center, Saitama, Japan, 4.Department of Human Genetics, Yokohama City University Graduate School of Medicine, Kanagawa, Japan)

Abstract password authentication.
Password is required to view the abstract. Please enter a password to authenticate.

Password