Department of Human Genetics, Yokohama City University Graduate School of Medicine, Fukuura, Kanazawa-ku, Yokohama, Japan.
Neurogenetics. 2012 Nov;13(4):327-32. doi: 10.1007/s10048-012-0337-6. Epub 2012 Jul 31.
Whole-exome sequencing of two affected sibs and their mother who showed a unique quadriceps-dominant form of neurogenic muscular atrophy disclosed a heterozygous DYNC1H1 mutation [p.H306R (c.917A>G)]. The identical mutation was recently reported in a pedigree with the axonal form of Charcot-Marie-Tooth disease. Three other missense mutations in DYNC1H1 were also identified in families with dominant spinal muscular atrophy with lower extremity predominance. Their clinical features were consistent with those of our family. Our study has demonstrated that the same DYNC1H1 mutation could cause spinal muscular atrophy as well as distal neuropathy, indicating pleotropic effects of the mutation.
对两名患病同胞及其母亲进行全外显子组测序,结果显示他们表现出一种独特的四头肌优势型神经源性肌肉萎缩,发现杂合 DYNC1H1 突变 [p.H306R (c.917A>G)]。最近在一个具有轴索型 Charcot-Marie-Tooth 病的家系中也报道了相同的突变。在以下肢为主的显性遗传性脊髓性肌萎缩症的家族中,还发现了 DYNC1H1 的另外三个错义突变。其他三个家族的临床特征与我们的家族一致。我们的研究表明,相同的 DYNC1H1 突变可导致脊髓性肌萎缩症和远端神经病,表明该突变具有多效性影响。