Dino Ferrari Center, Department of Pathophysiology and Transplantation, University of Milan, Milan, Italy.
Department of Neuroscience, Neurology Unit, IRCCS Foundation Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Ann Clin Transl Neurol. 2022 Nov;9(11):1820-1825. doi: 10.1002/acn3.51673. Epub 2022 Oct 25.
HTT full-penetrance pathogenic repeat expansions, the genetic cause of Huntington's disease (HD), have been recently reported in a minority of frontotemporal dementia/amyotrophic lateral sclerosis (ALS) patients (0.13%). We analyzed HTT CAG repeats in an Italian cohort of ALS patients (n = 467) by repeat-primed polymerase chain reaction. One patient harbored two expanded alleles in the HTT gene (42 and 37 CAG repeats). The absence of HD typical symptoms and the clinical picture consistent with ALS, corroborated by the diagnostic assessment, apparently excluded a misdiagnosis of HD.
HTT 全长穿透性致病重复扩展,亨廷顿病(HD)的遗传原因,最近在少数额颞叶痴呆/肌萎缩侧索硬化症(ALS)患者中报告(0.13%)。我们通过重复引物聚合酶链反应分析了意大利 ALS 患者队列(n=467)中的 HTT CAG 重复。一名患者在 HTT 基因中携带两个扩展等位基因(42 和 37 CAG 重复)。没有 HD 的典型症状和与 ALS 一致的临床图像,诊断评估得到证实,显然排除了 HD 的误诊。