Arsenault M-E, Prévost C, Lescault A, Laberge C, Puymirat J, Mathieu J
Neuromuscular Clinic, Carrefour de Santé de Jonquière, Quebec, Canada.
Neurology. 2006 Apr 25;66(8):1248-50. doi: 10.1212/01.wnl.0000208513.48550.08.
The authors report a genotype-phenotype correlation study in 102 patients with myotonic dystrophy type 1 carrying small CTG repeat expansions. Most patients carrying 50 to 99 CTG repeats were asymptomatic, except for cataracts. Myotonia, weakness, excessive daytime sleepiness, and myotonic discharges at EMG were significantly more present in the patients with 100 to 200 CTG repeats. These findings highlight different outcomes related to the expansion size, even among small CTG expansions.
作者报告了一项针对102例携带小CTG重复序列扩增的1型强直性肌营养不良患者的基因型-表型相关性研究。大多数携带50至99个CTG重复序列的患者无症状,仅患有白内障。携带100至200个CTG重复序列的患者中,肌强直、肌无力、日间过度嗜睡和肌电图显示的肌强直放电更为明显。这些发现突出了即使在小CTG扩增中,与扩增大小相关的不同结果。