The 59th Annual Meeting of the Japanese Society of Child Neurology

Session information

Poster Presentation

genetic abnormality

[P16] Poster Presentation
teratology 2

Thu. Jun 15, 2017 5:25 PM - 6:05 PM Poster (3F Event Hall)

Chair:Eiji Nanba(Center for Bioscience and Technology, Tottori, Japan)

Abe Chihiro1,2, Ayako Umemura1, Yuki Maki1, Naoko Kurahashi1, Keitaro Yamada1, Koichi Maruyama1, Kosaburo Aso1, Hirotomo Saitsu3 (1.Department of Pediatric Neurology, Aichi Prefectural Colony Central Hospital, Kasugai, Japan, 2.Department of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan, 3.Department of Biochemistry, Hamamatsu University School of Medicine, Hamamatsu, Japan)

Setsuri Yokoi1,2, Makiko Tsutsumi2, Fuyuki Miya3, Masafumi Miyata4, Mitsuhiro Kato5, Nobuhiko Okamoto6, Tatsuhiko Tsunoda3, Mami Yamasaki7, Yonehiro Kanemura8, Kenjiro Kosaki9, Shinji Saitoh10, Hiroki Kurahashi2 (1.Aichi Prefectural Aoitori Medical and Rehabilitation Center for Developmental Disabilities, Nagoya, Japan, 2.Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Japan, 3.Department of Medical Science Mathematics, Medical Research Institute, Tokyo Medical and Dental University, Tokyo, Japan, 4.Department of Pediatrics, Fujita Health University School of Medicine, Toyoake, Japan, 5.Department of Pediatrics, Showa University School of Medicine, Tokyo, Japan, 6.Department of Medical Genetics, Osaka Medical Center and Research Institute for Maternal and Child Health, Osaka, Japan, 7.Department of Pediatric Neurosurgery, Takatsuki General Hospital, Osaka, Japan, 8.Division of Regenerative Medicine, Institute for Clinical Research, Osaka National Hospital, National Hospital Organization, Osaka, Japan, 9.Center for Medical Genetics, Keio University School of Medicine, Tokyo, Japan, 10.Department of Pediatrics and Neonatology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan)

Mie Inaba1, Yukako Muramatsu1,2, Hiroko Taniai1,3, Norie Nonobe4, Hiroki Kurahashi5, Seiji Mizuno1 (1.Department of Pediatrics, Central Hospital Aichi Human Service Center, Aichi, Japan, 2.Department of pediatrics, Nagoya University, Aichi, Japan, 3.Central Care Center for Disabled Children City of Nagoya, Aichi, Japan, 4.Department of ophthalmology, Nagoya University, Aichi, Japan, 5.Division of Molecular Genetics Institute for Comprehensive Medical Science, Fujita Health University, Aichi, Japan)

Naoko Kurahashi1, Seiji Mizuno2, Mie Inaba2, Hirokazu Kurahashi3, Yuki Maki1, Chihiro Abe-hatano1, Keitaro Yamada1, Koichi Maruyama1, Masayo Kagami4, Kenji Kurosawa5, Miho Nakamura6 (1.Department of Pediatric Neurology, Aichi Prefectural Colony Central Hospital, Kasugai, Japan, 2.Department of Pediatrics, Aichi Prefectural Colony Central Hospital, Kasugai, Japan, 3.Department of Pediatrics, Aichi Medical University, Nagakute, Japan, 4.Department of Endocrinology and Metabolism, National Research Institute for Child Health and Development, Tokyo, Japan, 5.Division of Medical Genetics, Clinical Research Institute, Kanagawa Children's Medical Center, Yokohama, Japan, 6.Department of Functioning Science, Institute for Developmental Research, Aichi Human Service Center, Kasugai, Japan)