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Early recognition, diagnosis and treatment of spinal muscular atrophy

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Author:
No author available
Journal Title:
Chinese Journal of Pediatrics
Issue:
3
DOI:
10.3760/cma.j.cn112140-20221116-00976
Key Word:
No keyword available

Abstract: 脊髓性肌萎缩症(SMA)是一种常染色体隐性遗传性神经肌肉病,致病基因为SMN 1基因,以对称性进行性近端为主的肌无力为主要临床特征。近年来,SMA的分子致病机制研究及诊疗技术迅速发展,早期识别、及时诊断、规范治疗是临床实践的重点内容。

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