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在克鲁茨菲尔特-雅各布病的感觉障碍
Shmuel Appel1,2, Yael Cohen3, Shira Appel4
1Department of Neurology, Barzilai University Medical Center, Ashkelon, Israel. shmuela@barzi.health.gov.il.
概括
在遗传E200K克鲁茨菲尔特-雅各布病 (CJD) 中,感官症状更为频繁. 这些症状往往表明外周神经系统的参与,不同于典型的CJD表现.
科学领域:
- 神经科学是一个神经科学.
- 神经学 神经学
- 罕见疾病 罕见疾病
背景情况:
- 克鲁茨菲尔特-雅各布病 (CJD) 是一种致命的神经退行性疾病.
- 它的特点是迅速的痴呆,运动和精神衰退.
- 在CJD患者中偶尔会报告感官障碍.
研究的目的:
- 描述克鲁茨菲尔特-雅各布病的感官症状.
- 调查感官障碍的患病率和特征.
- 比较有和没有感官症状的CJD患者.
主要方法:
- 选了CJD以色列国家数据库的感官症状患者.
- 审查了症状特征,分布和人口/临床数据.
- 与有感觉症状的患者进行比较 (PNS与中枢神经系统参与).
主要成果:
- 在遗传E200KCJD中,感官症状更常见 (14.6%对5.6%).
- 麻木和神经病痛是最常见的,通常有"子手套"分布.
- 在有感官症状的患者中,有44%的患者观察到外围神经病变症状.
结论:
- 在E200KCJD中,感官症状更为普遍.
- 这些症状经常表明外周神经系统 (PNS) 的参与.
- 与不太频繁的经典EEG发现相关.
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