Methods The clinical data of 13 infants suffering from infantilespinalmuscularatrophy were analysed.
方法分析13例婴儿型脊髓性肌萎缩症患儿的临床资料。
2
Objective To investigate the clinical and electrophysiology features of infantilespinalmuscularatrophy, and explore the clinical significance of genetic diagnosis.
目的探讨婴儿型脊髓性肌萎缩症的临床、电生理特点及基因诊断的临床意义。
3
Infantile progressive spinalmuscularatrophy is an unusual motor neuron disease.