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克雅氏病(Creutzfeldt-Jakob disease)表现为球麻痹。

Creutzfeldt-Jakob disease presenting as bulbar palsy.

机构信息

Department of Neurology, The University of Kansas Medical Center, Kansas City, Kansas, USA.

出版信息

Muscle Nerve. 2010 Nov;42(5):833-5. doi: 10.1002/mus.21849.

DOI:10.1002/mus.21849
PMID:20976786
Abstract

Creutzfeldt-Jakob disease (CJD) is a degenerative neurological disorder caused by a prion protein. The diagnosis may be challenging in unusual early presentations. A bulbar symptom as the initial complaint is a rare presentation for CJD, with only a few reports so far. These patients can be misdiagnosed with motor neuron disease or the Miller Fisher variant of Guillain-Barré syndrome. We describe a 69-year-old woman with CJD who presented with bulbar symptoms at the onset.

摘要

克雅氏病(CJD)是一种由朊病毒蛋白引起的退行性神经疾病。在不常见的早期表现中,诊断可能具有挑战性。球部症状作为首发症状是 CJD 的罕见表现,迄今为止仅有少数报道。这些患者可能被误诊为运动神经元病或格林-巴利综合征的米勒-费舍尔变异型。我们描述了一位 69 岁女性,她以球部症状起病,患有 CJD。

相似文献

1
Creutzfeldt-Jakob disease presenting as bulbar palsy.克雅氏病(Creutzfeldt-Jakob disease)表现为球麻痹。
Muscle Nerve. 2010 Nov;42(5):833-5. doi: 10.1002/mus.21849.
2
[Psychiatric manifestations of a new variant of Creutzfeldt-Jakob disease. Apropos of a case].[新型克雅氏病的精神症状。附病例报告]
Encephale. 2001 Mar-Apr;27(2):194-7.
3
A Heidenhain variant of Creutzfeldt-Jakob disease: forensic implication.克雅氏病的海登海因变异型:法医学意义
Forensic Sci Int. 2004 Dec 2;146 Suppl:S51-4. doi: 10.1016/j.forsciint.2004.09.020.
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Creutzfeldt-Jakob disease with slow progression. A mimickry of progressive supranuclear palsy.进展缓慢的克雅氏病。一种进行性核上性麻痹的模仿病。
Bull Soc Sci Med Grand Duche Luxemb. 2007(2):125-30.
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Creutzfeldt-Jacob disease: an autopsy case report in tertiary care hospital.克雅氏病:一家三级医院的尸检病例报告
Indian J Pathol Microbiol. 2012 Jan-Mar;55(1):97-9. doi: 10.4103/0377-4929.94871.
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Creutzfeldt-Jakob disease: case report and review of the literature.克雅氏病:病例报告及文献综述
Acta Clin Croat. 2010 Jun;49(2):181-7.
7
Depressive disorder with psychotic symptoms as psychiatric presentation of sporadic Creutzfeldt-Jakob disease: a case report.以精神症状为表现的散发性克雅氏病的抑郁障碍:一例报告
Gen Hosp Psychiatry. 2006 Sep-Oct;28(5):452-4. doi: 10.1016/j.genhosppsych.2006.05.005.
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Sporadic Creutzfeldt-Jakob disease presenting with nonconvulsive status epilepticus.以非惊厥性癫痫持续状态为表现的散发性克雅氏病
Epilepsy Behav. 2004 Oct;5(5):792-6. doi: 10.1016/j.yebeh.2004.06.019.
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Familial Creutzfeldt-Jakob disease presenting as epilepsia partialis continua.表现为持续性部分性癫痫的家族性克雅氏病。
Epileptic Disord. 2008 Dec;10(4):271-5. doi: 10.1684/epd.2008.0216.
10
[Creutzfeldt-Jakob disease: a case that initiated with psychiatric symptoms].[克雅氏病:一例以精神症状起病的病例]
Turk Psikiyatri Derg. 2005 Spring;16(1):55-9.

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Sporadic Creutzfeldt-Jakob disease: Real-Time Quaking Induced Conversion (RT-QuIC) assay represents a major diagnostic advance.散发性 Creutzfeldt-Jakob 病:实时震颤诱导转化(RT-QuIC)检测法代表了主要的诊断进展。
Eur J Histochem. 2021 Oct 15;65(s1):3298. doi: 10.4081/ejh.2021.3298.
2
Creutzfeldt-Jakob disease with unusual presentation of peripheral neuropathy and ophthalmoplegia.具有周围神经病变和眼肌麻痹异常表现的克雅氏病
Avicenna J Med. 2018 Oct-Dec;8(4):153-156. doi: 10.4103/ajm.AJM_77_18.
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Isolated spasticity in sporadic Creutzfeldt-Jakob disease.
散发性克雅氏病中的孤立性痉挛
J Neurol. 2013 Feb;260(2):654-5. doi: 10.1007/s00415-012-6746-5. Epub 2012 Nov 16.