
| ID | 69878 |
| フルテキストURL | |
| 著者 |
Mitsutake, Akihiko
Department of Neurology, Graduate School of Medicine, The University of Tokyo
Osaki, Masao
Department of Neurology, Graduate School of Medicine, The University of Tokyo
Matsukawa, Takashi
Department of Neurology, Graduate School of Medicine, The University of Tokyo
Osako, Miho
Department of Neurology, Tokyo Metropolitan Kita Medical and Rehabilitation Center for the Disabled
Takeuchi, Chisen
Department of Neurology, Tokyo Metropolitan Kita Medical and Rehabilitation Center for the Disabled
Ishiura, Hiroyuki
Department of Neurology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences
Mitsui, Jun
Department of Precision Medicine Neurology, Graduate School of Medicine, The University of Tokyo
Kurokawa, Ryo
Department of Radiology, Graduate School of Medicine, The University of Tokyo
Mori, Harushi
Department of Radiology, School of Medicine, Jichi Medical University
Takahashi, Yuji
Department of Neurology, Graduate School of Medicine, The University of Tokyo
Goto, Jun
Department of Neurology, Graduate School of Medicine, The University of Tokyo
Tsuji, Shoji
Institute of Medical Genomics, International University of Health and Welfare
Toda, Tatsushi
Department of Neurology, Graduate School of Medicine, The University of Tokyo
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| 抄録 | Pathogenic variants in KIF1C cause Spastic Paraplegia 58 (SPG58), typically presenting with cerebellar ataxia and spastic paraparesis. We report two unrelated patients with spastic paraparesis, cerebellar ataxia, and tremor. Whole-exome sequence analysis identified novel homozygous variants in the motor domain of KIF1C (NM_006612.6): c.921G>A (p.Trp307Ter) and c.607C>T (p.Arg203Trp). In addition to the canonical brain MRI showing leukoencephalopathy with posterior dominance and hyperintensity along the corticospinal tracts, both patients showed symmetric T2 hyperintensity confined to the lateral and dorsal columns of the cervical cord. Given the long disease durations (22 and 51 years), these findings may represent late-emerging or previously overlooked spinal cord involvement and broaden the neuroradiological spectrum of SPG58.
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| キーワード | cerebellar ataxia
hereditary spastic paraplegia
KIF1C
leukoencephalopathy
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| 発行日 | 2025-11-14
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| 出版物タイトル |
Annals of Clinical and Translational Neurology
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| 出版者 | Wiley
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| ISSN | 2328-9503
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| 資料タイプ |
学術雑誌論文
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| 言語 |
英語
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| OAI-PMH Set |
岡山大学
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| 著作権者 | © 2025 The Author(s).
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| 論文のバージョン | publisher
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| DOI | |
| Web of Science KeyUT | |
| 関連URL | isVersionOf https://doi.org/10.1002/acn3.70248
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| ライセンス | http://creativecommons.org/licenses/by/4.0/
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| Citation | A. Mitsutake, M. Osaki, T. Matsukawa, et al., “ Dorsolateral Cervical Cord T2 Hyperintensity in KIF1C-Related Disease (Spastic Paraplegia 58): Two Long-Duration Cases,” Annals of Clinical and Translational Neurology (2025): 1–6, https://doi.org/10.1002/acn3.70248.
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