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表现为运动神经元病的亨廷顿舞蹈症。

Huntington chorea presenting with motor neuron disease.

作者信息

Sadeghian Hamid, O'Suilleabhain Padraig E, Battiste James, Elliott Jeffrey L, Trivedi Jaya R

机构信息

Department of Neurology, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX 75390-8897, USA.

出版信息

Arch Neurol. 2011 May;68(5):650-2. doi: 10.1001/archneurol.2011.76.

Abstract

BACKGROUND

There have been a few case reports of motor neuron disease in association with Huntington disease (HD).

OBJECTIVE

To describe a patient presenting with prominent fasciculations, chorea, and possible amyotrophic lateral sclerosis (ALS) in whom genetic testing revealed HD mutation.

DESIGN

Case report.

SETTING

University of Texas Southwestern Medical Center, Dallas. Patient  A 69-year-old man with chorea and fasciculations.

INTERVENTIONS

Genetic and electrophysiologic testing.

MAIN OUTCOME MEASURES

Genetic test result, electrophysiologic test result, and physical examination.

RESULTS

A 69-year-old man with long-standing depression and failing memory presented with muscle twitches of 8 months' duration. He was found to have choreoathetoid movements and distal weakness on neurological examination. Electrophysiologic studies revealed evidence of motor neuron disease. Genetic test showed CAG repeat of 40 on chromosome 4, confirming the diagnosis of HD.

CONCLUSION

Motor neuron disease can rarely occur in patients with HD and could be one of its presenting features.

摘要

背景

已有少数运动神经元病与亨廷顿病(HD)相关的病例报告。

目的

描述一名出现明显肌束震颤、舞蹈症及可能的肌萎缩侧索硬化(ALS)的患者,其基因检测显示存在HD突变。

设计

病例报告。

地点

达拉斯的德克萨斯大学西南医学中心。患者为一名69岁有舞蹈症和肌束震颤的男性。

干预措施

基因和电生理检测。

主要观察指标

基因检测结果、电生理检测结果及体格检查。

结果

一名患有长期抑郁症且记忆力减退的69岁男性出现了持续8个月的肌肉抽搐。神经科检查发现他有舞蹈徐动症样运动和远端无力。电生理研究显示存在运动神经元病的证据。基因检测显示4号染色体上CAG重复序列为40,确诊为HD。

结论

运动神经元病在HD患者中很少见,且可能是其首发特征之一。

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