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

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English Session

genetic abnormality

[E5] English Session 5
genetic disorder

Fri. Jun 16, 2017 8:50 AM - 9:50 AM Room No.6 (10F Conference Room 1009)

Chair:Yoshiko Nomura（Yoshiko Nomura Neurological Clinic for Children, Tokyo, Japan）, Toshiyuki Yamamoto（Institute of Medical Genetics, Tokyo Women’s Medical University, Tokyo, Japan）

[E-031] A boy with myoclonus dystonia syndrome diagnosed by whole exome sequencing

○Akihiko Miyauchi1, Ayumi Matsumoto1, Masako Nagashima1, Yukifumi Monden1, Noriko Oguro2, Haruo Shintaku3, Yuri Uchiyama4, Mitsuko Nakashima4, Naomichi Matsumoto4, Hitoshi Osaka1, Takanori Yamagata1 (1.Department of Pediatrics, Jichi Medical University, Tochigi, Japan, 2.Department of Pediatrics, Tochigi Rehabilitation Center, Tochigi, Japan, 3.Department of Pediatrics, Osaka City University Graduate School of Medicine, Osaka, Japan, 4.Department of Human Genetics, Yokohama City University Graduate School of Me dicine, Kanagawa, Japan)

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