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表现为运动神经元病的马查多-约瑟夫病

Machado-Joseph disease presenting as motor neuron disease.

作者信息

Pinto Susana, De Carvalho Mamede

机构信息

Neuromuscular Unit, Institute of Molecular Medicine, Faculty of Medicine, University of Lisbon, Portugal.

出版信息

Amyotroph Lateral Scler. 2008 Jun;9(3):188-91. doi: 10.1080/17482960701702603.

Abstract

Machado-Joseph disease (MJD) is a spinocerebellar degeneration with a wide phenotypic presentation. A 64-y-old male with a history of gait disability and fasciculations was referred to our unit with the diagnosis of motor neuron disease (MND), which was supported by the presence of upper motor neuron signs and diffuse loss of motor units on electromyography. Trunk and cranial-innervated muscles were clearly affected. Respiratory function was mildly affected. Cerebellar ataxia developed over time and the diagnosis of MJD was confirmed by genetic studies. MJD should be considered in the differential diagnosis of MND.

摘要

马查多-约瑟夫病(MJD)是一种具有广泛表型表现的脊髓小脑变性疾病。一名64岁男性,有步态障碍和肌束震颤病史,因运动神经元病(MND)诊断被转诊至我院,上运动神经元体征及肌电图显示运动单位广泛丢失支持该诊断。躯干和由脑神经支配的肌肉明显受累。呼吸功能轻度受损。随着时间推移出现小脑共济失调,基因研究确诊为MJD。在MND的鉴别诊断中应考虑MJD。

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