関連する実験動画
Updated: Sep 9, 2025

Modeling Myotonic Dystrophy 1 in C2C12 Myoblast Cells
Published on: July 29, 2016
ミオトニク・ディストロフィー タイプ 1 の 診断 に つながる アファシア: 症例 報告
Shinichiro Maeshima1, Akinori Takeda2, Keita Sakurai3
1Education and Innovation Center, National Center for Geriatrics and Gerontology, Obu, JPN.
この症例は,ミオトニック・ディストロフィー1型 (DM1) の希少な初期症状としての進行性アファシアを強調しています. 筋肉縮による非典型的失語症の早期発見は,この多システム障害の診断に不可欠です.
科学分野:
- 神経学
- 遺伝学
背景:
- ミオトニク・ディストロフィー1型 (DM1) は,通常,ミオトニクと筋肉の弱さで表れる多系統性疾患である.
- 中枢神経系 (CNS) の関与は認められていますが,最初の症状として言語障害はまれです.
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08:07Single Myofiber Isolation and Culture from a Murine Model of Emery-Dreifuss Muscular Dystrophy in Early Post-Natal Development
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