[P50] Muscular disease

Fri. Jun 1, 2018 5:10 PM - 5:40 PM Poster (Convention Hall A)

Chair: Akihiko ISHIYAMA(Department of Child Neurology, National Center Hospital, National Center of Neurology and Psychiatry)

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[P-286] Two Duchenne muscular dystrophy patients with cerebral infarction

Fumihito Nozaki, Tomohiro Kumada, Minoru Shibata, Kenji Inoue, Saeko Sasaki, Anri Hayashi, Tatsuya Fujii (Department of Pediatrics, Shiga Medical Center for Children, Moriyama, Shiga)

[P-287] A study of the association between scoliosis and the age of ambulatory loss in dystrophinopathy

Terumi Murakami^1,2, Takuhisa Tamura¹, Mikiya Suzuki¹, Kazunari Monma¹, Toshiki Shigeyama³, Sachiko Namatame¹, Yuka Wakabayashi¹, Kouhei Morimoto¹, Kana Yatabe¹, Katsuhisa Ogata¹ (1.Department of Neurology, National Hospital Organization Higashisaitama Hospital, Saitama, Japan, 2.Department of Pediatrics, Tokyo Women's Medical University, Tokyo, Japan, 3.Department of Cardiology, National Hospital Organization Higashisaitama Hospital, Saitama, Japan)

[P-288] A severe LMNA—related congenital muscular dystrophy caused by a novel mutation

Lee Tomoko¹, Hideki Shimomura¹, Chikako Mure¹, Maiko Misaki¹, Tsubasa Koda¹, Akio Shibata¹, Kumi Kawamoto¹, Yoko Okada², Makoto Koizumi², Kyoko Ito³, Yasuhiro Takashima¹ (1.Department of pediatrics, Hyogo College of Medicine, Nishinomiya, Japan, 2.Department of pediatrics, Hyogo Prefectural Nishinomiya Hospital, Nishinomiya, Japan, 3.Department of Pathology and Applied neurobiology Graduate School of Medical Science Kyoto Prefectural University of Medicine, Kyoto, Japan)

[P-289] A case of CFTD with progressive cerebellar atrophy presented a diagnostic difficulty

Sadao Nakamura¹, MAKI TOYMA¹, YUIKO HAMADA¹, YASUTUGU CHINEN¹, ICHIZO NISHINO², KOICI NAKANISHI¹ (1.Department of Pediatrics, Faculty of Medicine, University of the Ryukyus, Okinawa, Japan, 2.Department of Neuromuscular Research, National Center of Neurology and Psychiatry, Tokyo, Japan)

[P-290] An early treatment for rhabdomyolysis by viral infection in Fukuyama congenital muscular dystrophy

Hirokazu Takechi¹, Atsuko Oba¹, Kenjiro Kikuchi², Yasuyuki Wada¹ (1.The Jikei University Kashiwa Hospital, 2.The Jikei University School of Medicine Department of Pediatrics)

[P-291] A case of severe dilated cardiomyopathy caused by compound heterozygous of FKTN gene point mutations

Naoko Shiba^1,2, AKINORI NAKAMURA^3,4, TETSUO OZAWA^5,6, KAZUHIRO KIMURA⁷, HIROHIKO MOTOKI⁷, KOICHIRO KUWAHARA⁷, MASARU NASUNO², SHIHOKO TAKEUCHI², TAKENORI NATSUME², TOSHIMITSU YANAGISAWA², MITSUO MOTOBAYASHI², TETSUHIRO FUKUYAMA⁸, YUJI INABA⁸ (1.Regenerative Science and Medicine, Shinshu University, Matsumoto, Japan, 2.Department of Pediatrics, Shinshu University, Matsumoto, Japan, 3.The third department of Medicine, Shinshu University, Matsumoto, Japan, 4.Department of Neurology, National Hospital Organization Matsumoto Medical Center)