Infantile progressive spinal muscular atrophy is an unusual motor neuron disease.
婴儿型进行性脊肌萎缩症是一种少见的运动神经元性疾病。
2
Objective To investigate the clinical and electrophysiology features of infantile spinal muscular atrophy, 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
Methods The clinical data of 13 infants suffering from infantile spinal muscular atrophy were analysed.