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

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English Session

Hereditary disorder

[E3] English Session 3
Hereditary disorder

Fri. Jun 1, 2018 9:50 AM - 10:50 AM Room 8 (1F 103)

Chair:Mitsuhiro Kato（ Department of Pediatrics, Showa University School of Medicine,　Tokyo, Japan）,　Toshiyuki Yamamoto（ Institute of Medical Genetics, Tokyo Womens Medical University,　Tokyo, Japan）

[E-011] HECW2 mutation causes peculiar periodic attacks of paralysis, intellectual disability and hypotonia

Kazuyuki Nakamura1, Mitsuhiro Kato1, 2, Takahiro Abiko1, Takashi Kanbayashi3, Mitsuko Nakashima4, 5, Hirotomo Saitsu4, 5, Naomichi Matsumoto5 (Department of Pediatrics, Yamagata University Faculty of Medicine, Yamagata, Japan1, Department of Pediatrics, Showa University School of Medicine, Tokyo, Japan2, Department of Psychiatry, Akita University Graduate School of Medicine, Akita, Japan3, Department of Biochemistry, Hamamatsu University School of Medicine, Hamamatsu, Japan4, Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan5)

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