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强直性肌营养不良症中的多模态诱发电位

Multimodality evoked potentials in myotonic dystrophy.

作者信息

Sartucci F, Marconi F, Busso E, Rossi B, Murri L

机构信息

Istituto di Clinica Neurologica, Università di Pisa.

出版信息

Ital J Neurol Sci. 1989 Feb;10(1):61-7. doi: 10.1007/BF02333873.

Abstract

Multimodality evoked potentials were performed in 18 patients affected by myotonic dystrophy (8 males and 10 females); the aim was to make an electrophysiological evaluation of the central nervous system involvement in this disease. We observed brainstem, somatosensory and visual evoked potential abnormalities respectively in 53%, 62.5% and 71.4% of cases, with no apparent relationship to the severity of the disease. Our abnormal findings provide further confirmation of CNS involvement in myotonic dystrophy and occur in various combinations suggesting an aspecific involvement at different levels, reflecting the multisystemic character of this disease.

摘要

对18例强直性肌营养不良患者(8例男性,10例女性)进行了多模态诱发电位检查;目的是对该疾病中中枢神经系统受累情况进行电生理评估。我们分别在53%、62.5%和71.4%的病例中观察到脑干、体感和视觉诱发电位异常,这些异常与疾病严重程度无明显关系。我们的异常发现进一步证实了中枢神经系统受累于强直性肌营养不良,且以各种组合形式出现,提示在不同水平存在非特异性受累,反映了该疾病的多系统特征。

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