Corcia P, Khoris J, Couratier P, Mayeux-Portas V, Bieth E, De Toffol B, Autret A, Müh J P, Andres C, Camu W
INSERM U316, Tours, France.
Neurology. 2002 Nov 12;59(9):1464-6. doi: 10.1212/01.wnl.0000032500.73621.c5.
Spinal muscular atrophy (SMA) is caused by SMN1 gene deletions or mutations, and ALS is the most frequent motor neuron condition in adults. The authors describe three families in which ALS and SMA coexist. The authors found that no SOD1 mutation was found within these families; all three ALS cases had at least two SMN1 copies; and an abnormal SMN1 gene locus did not explain the co-occurrence of these two motor neuron disorders in these families.
脊髓性肌萎缩症(SMA)由SMN1基因缺失或突变引起,而肌萎缩侧索硬化症(ALS)是成人中最常见的运动神经元疾病。作者描述了三个ALS和SMA共存的家族。作者发现,这些家族中未发现SOD1突变;所有三例ALS病例均至少有两个SMN1拷贝;并且异常的SMN1基因位点并不能解释这两个家族中这两种运动神经元疾病的共存情况。