丘脑切开术
医学
神经系统疾病
脑病
物理医学与康复
线粒体脑肌病
运动障碍
中枢神经系统疾病
外科
脑深部刺激
麻醉
帕金森病
疾病
内科学
基因
化学
突变
生物化学
作者
Norbert Kovács,Endre Pál,István Balás,József Janszky,Ferenc Nagy,Hajnalka Merkli
摘要
Abstract A 53‐year‐old woman underwent several ischemic stroke‐like episodes and later developed incomplete, bilateral ophthalmoplegia, left vision deterioration, and bilateral tremor. The clinical course, laboratory data, and muscle histology led to a diagnosis of mitochondrial encephalomyopathy. No other etiology could be identified in the background of her disabling bilateral postural–kinetic tremor. As this tremor did not respond to pharmacological therapy, left thalamotomy and subsequently right thalamic deep brain stimulator (DBS) implantation were performed, which resulted in an excellent clinical outcome. The Fahn–Tolosa–Marin Tremor Rating Scale improved from 110 to 11 points. This case suggests that the rare tremor caused by mitochondrial encephalopathy may be treated long‐term with either thalamotomy or thalamic DBS implantation. © 2006 Movement Disorder Society
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