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婴儿型脊髓性进行性肌萎缩是较少见的神经肌肉系统遗传疾病,以进行性肌萎缩及弛缓性瘫痪为特征。我们于1986年12月收治兄弟二人同患此病,殊为少见,报告如下。
Infantile spinal progressive muscular atrophy is a rare genetic disease of the neuromuscular system characterized by progressive amyotrophy and flaccid paralysis. We admitted in December 1986 two brothers suffering from the disease, are rare, the report is as follows.