Japanese Poster Session

[Pj-111] Peripheral neuropathy (CMT)

Sat. May 25, 2019 1:15 PM - 2:30 PM Poster Exhibition (Osaka International Convention Center 3F Event Hall)

Chair:Eiji Matsuura(Department of neurology and geriatrics, Kagoshima University Graduate School of Medical and Dental Sciences)

+Add all to schedule

[Pj-111-1] Clinical analysis of hereditary peripheral neuropathy with MPZ mutation

Takaki Taniguchi¹, Akiko Yoshimura¹, Masahiro Ando^1,2, Yu Hiramatsu^1,3, Hajime Tanabe¹, Yujiro Higuchi¹, Tomonori Nakamura¹, Yusuke Sakiyama¹, Akihito Hashiguchi¹, Yuji Okamoto¹, Eiji Matsuura¹, Hiroshi Takashima¹ (1.Department of Neurology and Geriatrics, Kagoshima University Graduate School of Medical and Dental Sciences, 2.Kikuno Hospital, 3.Ogura Hospital)

[Pj-111-2] Charcot-Marie-Tooth disease type2B with a novel Rab7variant showing different phenotypes in a family

Yasutake Tada¹, Kenji Sakai¹, Ryoichi Takahashi¹, Hiroki Yamaguchi¹, Miharu Samuraki¹, Tsuyoshi Hamaguchi¹, Akihiro Hashiguchi², Hiroshi Takashima², Masahito Yamada¹ (1.Departmet of Neurology and Neurobiology of Aging, Kanazawa University Graduate School of Medical Science, 2.Department of Neurology and Geriatrics, Kagoshima University Graduate School of Medical and Dental Sciences)

[Pj-111-3] The study of CMT1A with hyperCKemia

Suguru Takeshita, Naoki Takegami, Ayako Koguchi, Akatuki Kubota, Hiroyuki Ishiura, Naohiro Uchio, Atushi Unuma, Aya Kamisawa, Tatuo Mano, Yu Nagashima, Yuuichirou Shirota, Masashi Hamada, Kaori Sakuishi, Jun Shimizu, Tatushi Toda (Department of Neurology, The University of Tokyo Hospital)

[Pj-111-4] CMT1A and Waardenburg syndrome type 2 -"Double trouble" in hereditary neuropathy -

Nozomu Matsuda¹, Koushi Ootsuki², Shunsuke Kobayashi¹, Ayaka Nemoto³, Hitoshi Kubo³, Shinichi Usami⁵, Yoshikazu Ugawa^1,4, Kazuaki Kanai¹ (1.Department of Neurology, Fukushima Medical University, 2.Department of Otorhinolaryngology, Fukushima Medical University, 3.Advanced Clinical Research Center, Fukushima Medical University, 4.Department of Neuro-Regeneration, Fukushima Medical University, 5.Department of Otorhinolaryngology, Shinshu University School of Medicine)

[Pj-111-5] Identification of MME and COA7 as two novel causative genes for inherited peripheral neuropathy

Yujiro Higuchi¹, Akihiro Hashiguchi¹, Junhui Yuan¹, Akiko Yoshimura¹, Yuji Okamoto¹, Eiji Matsuura¹, Hayato Yabe², Takehiro Ueda³, Takashi Koide⁴, Hiroaki Yaguchi⁵, Jun Mitsui⁶, Hiroyuki Ishiura⁶, Masanori Nakagawa⁷, Shinichi Morishita⁸, Tatsushi Toda^3,6, Shoji Tsuji⁶, Hiroshi Takashima¹ (1.Department of Neurology, Kagoshima University Hospital, 2.Clinical Pharmacology, Ehime University Graduate School of Medicine, 3.Department of Neurology, Kobe University Graduate School of Medicine, 4.Department of Neurology, Hiratsuka City Hospital, 5.Department of Neurology, Brain Center, Sapporo City General Hospital, 6.The University of Tokyo Hospital, 7.North Medical Center, Kyoto Prefectural University of Medicine, 8.Department of Computational Biology and Medical Sciences, Graduate School of Frontier Sciences, The University of Tokyo)