1) spinoneural atrophy
脊髓神经性肌萎缩;变性萎缩
2) 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。
3) Spinal muscular atrophy
脊髓性肌萎缩症
1.
Quantitative studies on SMN1 gene and carrier testing of spinal muscular atrophy;
脊髓性肌萎缩症SMN1基因定量研究及基因携带者的筛查(英文)
2.
Rapid diagnosis of spinal muscular atrophy using denaturing high-performance liquid chromatography;
应用变性高效液相色谱技术快速诊断儿童型脊髓性肌萎缩症(英文)
3.
Prenatal diagnosis of spinal muscular atrophy based on umbilical cord blood;
胎儿脐带血产前诊断脊髓性肌萎缩症
5) 5qSMA
5q脊髓性肌萎缩
6) 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。
补充资料：肌萎缩性脊髓侧索硬化
肌萎缩性脊髓侧索硬化
amyotrophic〖JP〗lateral sclerosis
一种原因未明的进行性的神经系统变性疾病，可能与遗传、中毒、损伤、感染有关。突出的病理变化为皮质延髓束和皮质脊髓束的变性，脊髓前角细胞以及脑干运动神经核的损害，锥体束的变性最早出现在脊髓比较低的部位，随病程进展，逐渐向高位脊髓及脑干推进。患者可有麻木和发凉等感觉异常，肌肉无力、挛缩、肌束颤动及萎缩、持久性腱反射亢进和病理反射，随时间增长，无力症状扩展到躯干及颈部，最后累及面部及延髓支配的肌肉，出现其相应症状和体征。无特殊治疗。
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