Amyotrophic lateral sclerosis - a motor neuron disease. Case report

被引:0
作者
Rubinowicz-Zasada, Maja [1 ]
Orczyk, Aneta [2 ]
Orczyk, Marek [2 ]
Pasek, Jaroslaw [3 ]
机构
[1] Jerzy Kukuczka Acad Phys Educ Katowice, Dept Physiotherapy Dis Internal Organs, Katowice, Poland
[2] Univ Dabrowa Gornicza, Fac Physiotherapy, Dept Pedag, Dabrowa Gornicza, Poland
[3] Med Univ Katowice, Ctr Diag & Laser Therapy Bytom, Sch Med, Dept & Clin Ward Internal Dis Angiol & Phys Div D, Stefana Batorego 15, PL-41902 Bytom, Poland
来源
PEDIATRIA I MEDYCYNA RODZINNA-PAEDIATRICS AND FAMILY MEDICINE | 2015年 / 11卷 / 01期
关键词
ALS; amyotrophic lateral sclerosis; fasciculation; motor neuron disease;
D O I
10.15557/PiMR.2015.0010
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Amyotrophic lateral sclerosis, also known as Charcot's disease and motor neuron disease, is a progressive neurodegenerative disease that causes muscle weakness, paralysis, and ultimately, respiratory failure. The aetiology and the pathogenesis of the syndrome remain unknown. Most people live 2-5 years after their first signs of the disease. There is no cure or effective treatment. We present a case of a female patient affected by progressing Charcot's disease. On the Amyotrophic Lateral Sclerosis Functional Rating Scale - Revised (ALSFRS-R), the patient obtained 21 points. Atrophy and muscle spasm were very extended. Electromyography revealed features of coexisting denervation and reinnervation in the examined muscles. A growing number of Charcot's disease cases require multidirectional actions to meet patient's physical, emotional, and nutritional needs. Amyotrophic lateral sclerosis is an incurable disease. However, it is possible to relieve its symptoms by applying systematic physical rehabilitation.
引用
收藏
页码:112 / 118
页数:7
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