肌张力障碍
医学
帕金森病
左旋多巴
脊髓小脑共济失调
共济失调
运动障碍
运动障碍
小脑共济失调
神经系统疾病
儿科
物理医学与康复
中枢神经系统疾病
帕金森病
外科
内科学
精神科
疾病
作者
Jun Ikezawa,Rui Shimazaki,Shinsuke Tobisawa,Kimio Sugaya,Kazushi Takahashi
标识
DOI:10.1016/j.clineuro.2023.107721
摘要
Spinocerebellar ataxia 6 (SCA6) often presents with pure cerebellar ataxia. It is rarely accompanied by extrapyramidal symptoms, such as dystonia and parkinsonism. Here, we describe a case of SCA6 with dopa-responsive dystonia for the first time. A 75-year-old woman was admitted to the hospital with slowly progressive cerebellar ataxia and dystonia in the left upper limb for the past six years. Genetic testing confirmed the diagnosis of SCA6. Her dystonia improved with oral levodopa, and she was able to raise her left hand. Oral levodopa administration may provide early-phase therapeutic benefits for SCA6-associated dystonia.
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