[P16] Epilepsy/Convulsion Diagnosis/Gene

[P-091] Two cases of absence epilepsy caused by SYNGAP1 mutations

Yu Kobayashi¹, TAKAO KOMATSUBARA¹, MOEMI HOJO¹, SHINICHI MAGARA¹, JUN TOHYAMA¹, MITSUHIRO KATO², MITSUKO NAKASHIMA³, NAOMICHI MATSUMOTO⁴ (1.Department of Child Neurology, Nishi-Niigata Chuo National Hospital, Niigata, Japan, 2.Department of Pediatorics, Showa University School of Medicine, Tokyo, Japan, 3.Department of Biochemistry, Hamamatsu University School of Medicine, Hamamatsu, Japan, 4.Department of Human Genetics, Yokohama City University Graduate School of Me dicine, Yokohama, Japan)