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The Coexistence of Multiple Sclerosis and Hereditary Spastic Paraparesis in a Patient

机译:多发性硬化症和遗传性痉挛性轻瘫的并存

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摘要

Multiple sclerosis (MS) is a chronic disease characterized by multiple areas of central nervous system inflammation, demyelination and axonal loss. Hereditary spastic paraparesis (HSP) is characterized clinically by progressive spasticity and weakness of the lower limbs and pathologically by retrograd axonal degeneration of the corticospinal tracts and posterior columns. We identified a patient with clinical history and investigation findings consistent with the concurrence of both MS and HSP. Laboratory and radiological investigations, cognitive tests were performed. Genetic confirmation for spastin gene mutation has been completed. If this coexistence is not coincidence the mutation in the spastin gene may be a strong susceptibility locus for MS.
机译:多发性硬化症(MS)是一种慢性疾病,其特征在于中枢神经系统发炎,脱髓鞘和轴突丢失的多个区域。遗传性痉挛性轻瘫(HSP)在临床上以下肢进行性痉挛和无力为特征,病理上以皮质脊髓束和后柱的逆行轴突变性为特征。我们确定了一名患者,其临床病史和调查结果与MS和HSP的并发一致。进行实验室和放射学调查,进行认知测试。 spastin基因突变的遗传确认已经完成。如果这种共存不是巧合,那么spastin基因中的突变可能是MS的强烈易感基因座。

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