1) myotonia atrophica
萎缩性肌强直
2) myotonic atrophy
肌强直性萎缩
3) myopathic atrophy
肌病性萎缩
4) neuralgic amyotrophy
神经痛性肌萎缩
1.
Objective To investigate the clinical features and characteristic of auxiliary examination of neuralgic amyotrophy(NA).
目的探讨神经痛性肌萎缩的临床及辅助检查特点。
2.
ObjectiveTo investigate the clinical features and nursing care of neuralgic amyotrophy.
目的探讨神经痛性肌萎缩的临床及护理特点。
5) benign calf amyotrophy
良性腓肠肌萎缩
6) Spinal muscular atrophy
脊髓性肌萎缩
1.
Objective Spinal muscular atrophy (SMA) is one of common autosomal recessive diseases and is characterized by degeneration of the anterior horn cells of the spinal cord.
目的脊髓性肌萎缩(spinal muscular atrophy,SMA)是以脊髓前角运动神经元退化变性为特征的一种常见的常染色体隐性遗传病。
2.
Objective To establish a gene diagnosis assay for spinal muscular atrophy(SMA) in children.
目的探讨儿童脊髓性肌萎缩症(SMA)的特异性基因诊断方法。
补充资料：萎缩性肌强直症
萎缩性肌强直症
病名。即肌紧张性营养不良综合征。详见该条。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条