脊髓性肌萎缩是一种神经系统遗传性疾病,其婴儿型又称为Werdnig-Hoffmann氏病,现将我们所见1例报告如下。 患者,男,2岁5个月,因全身软弱无力2年余,发热咳嗽3天,于1984年4月入院。患儿为第一胎,足月顺产。其父母为非近亲配偶,家族中无同样 Spinal muscular atrophy is a genetic disease of the nervous system, its infantile type is also known as Werdnig-Hoffmann’s disease, now we see a report of the following. Patients, male, 2 years and 5 months, due to systemic weakness more than 2 years, fever, cough for 3 days, in April 1984 admitted. Children for the first child, full-term birth. Their parents are non-relatives of spouses, not the same family