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为了进一步了解和认识某些神经原性肌萎缩的特点,特别是不同类型肌纤维的病变情况,以利于早期诊断。为此,本文对日本东北大学医学部脑研神经内科25例神经原性肌萎缩肌肉活检标本,采取形态计测的方法进行研究观察,拟报告如下。资料和方法本组共25例神经原性肌萎缩,其中SMA5例、ALS4例,其中CPK高值的MND3例(ALS2例、SMA1例),KAS5例,亚急性神经病4例(SLE1例,Crow-Fukase Syndrome 2例,中毒性神经病
In order to further understand and recognize some neurogenic muscle atrophy characteristics, especially the different types of muscle fiber lesions, in order to facilitate early diagnosis. To this end, this article on the Japanese Department of Neurology, Department of Neurology, Northeastern University, 25 cases of neurogenic muscular atrophy muscle biopsy specimens to take the form of measurement methods to observe the study, to be reported as follows. Materials and Methods The group of 25 cases of neurogenic muscle atrophy, including 5 cases of SMA, 4 cases of ALS, CPK high value of MND3 cases (ALS2 cases, SMA1 cases), KAS5 cases, subacute neuropathy in 4 cases (SLE1 cases, Crow- 2 cases of Fukase Syndrome, toxic neuropathy