在肌缩侧面硬化症的dysautonomia
Alexandra L Oprisan1,2, Bogdan Ovidiu Popescu1,2,3
1Department of Clinical Neurosciences, Carol Davila University of Medicine and Pharmacy, 020021 Bucharest, Romania.
International journal of molecular sciences
|October 14, 2023
概括
肌缩侧面硬化症 (ALS) 是一种复杂的神经退行性疾病. 本综述探讨了ALS患者经常被低估的自主神经系统障碍,强调了需要更多的研究.
科学领域:
- 神经科学是一个神经科学.
- 神经学 神经学
- 自主性功能障碍 自主性功能障碍
背景情况:
- 肌缩侧面硬化症 (ALS) 是一种进展性神经退行性疾病,主要影响运动神经元.
- 越来越多的人认为ALS是一种多系统性疾病,具有显著的遗传,临床和神经病理异质性.
- 包括自主功能障碍在内的非运动症状存在,但在ALS中经常被低估.
研究的目的:
- 进行关于ALS患者自主性障碍的叙事文献综述.
- 综合现有关于自主神经系统参与ALS的数据.
- 突出目前在这种特殊的ALS领域研究的稀缺性.
主要方法:
- 叙事文学评论. 叙事文学评论. 叙事文学评论. 叙事文学评论.
- 对评估自主神经系统参与ALS的现有研究进行分析.
- 来自稀缺可用的研究数据的综合.
主要成果:
- 在患有ALS的患者中记录了自主症状和症状.
- 用各种分析方法来评估ALS中自主神经系统的功能.
- 关于ALS中自主性障碍的数据仍然有限.
结论:
- 自主功能障碍是ALS的一个特征,有助于其作为多系统疾病的复杂性.
- 进一步的研究至关重要,以全面了解和解决ALS的自主性障碍.
- 增加对自主参与的认可可能会改善患者护理和管理策略.
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