进行性肌萎缩
肌萎缩侧索硬化
肌萎缩
运动神经元
萎缩
医学
下运动神经元
神经科学
病理
物理医学与康复
心理学
疾病
作者
Jeldican Visser,J.M.B.V. de Jong,Marianne de Visser
出处
期刊:Neurology
[Lippincott Williams & Wilkins]
日期:2008-02-25
卷期号:70 (9): 723-727
被引量:34
标识
DOI:10.1212/01.wnl.0000302187.20239.93
摘要
Since its first description more than a century ago, there has been much debate about the diagnostic entity progressive muscular atrophy (PMA). Initially, PMA included all forms of progressive amyotrophy. With the identification of several myogenic and neurogenic diseases and the recognition of amyotrophic lateral sclerosis (ALS), PMA was deemed to disappear as a nosologic entity at the end of the 19th century. In the last century, various other lower motor neuron syndromes were distinguished which may previously have been designated as cases of PMA. In contrast, several observations provided evidence that PMA can be linked both clinically and pathologically to ALS. Therefore, PMA should be considered as a syndromal subtype within a clinical spectrum of motor neuron diseases.
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