Machado-Joseph disease presenting as motor neuron disease

被引:13
作者
Pinto, Susana [2 ]
De Carvalho, Mamede [1 ,2 ]
机构
[1] Hosp Santa Maria, Dept Neurol, Lisbon, Portugal
[2] Univ Lisbon, Fac Med, Inst Mol Med, Neuromuscular Unit, P-1699 Lisbon, Portugal
来源
AMYOTROPHIC LATERAL SCLEROSIS | 2008年 / 9卷 / 03期
关键词
amyotrophic lateral sclerosis; Machado-Joseph disease; motor neuron disease; spinocerebellar ataxia type-3;
D O I
10.1080/17482960701702603
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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.
引用
收藏
页码:188 / 191
页数:4
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