Serratrice G
Rev Neurol (Paris). 1985;141(4):322-4.
Familial cases of A.L.S. are more frequent in young people. The course is short. There are some alterations of sensory pathways. However some atypical cases are known. Three patients had such clinical features: in the first case there was a progressive weakness of scapular girdle with neck muscles involvement. The second case was a progressive spinal amyotrophy. The last was a bulbar form. In all 3 cases there was an autosomal dominant inheritance, but the course was slow.
肌萎缩侧索硬化症（A.L.S.）的家族性病例在年轻人中更为常见。病程较短。感觉通路存在一些改变。然而，也有一些非典型病例。三名患者具有以下临床特征：第一例患者肩胛带进行性无力，并累及颈部肌肉。第二例是进行性脊髓性肌萎缩。最后一例是延髓型。所有这三例均为常染色体显性遗传，但病程缓慢。
