Altıner Şule, Ardic Senol, Çebi Alper H
Department of Medical Genetics, Trabzon Kanuni Training and Research Hospital, University of Health Sciences, Trabzon, Turkey.
Department of Emergency Medicine, Faculty of Medicine, University of Health Sciences, Trabzon, Turkey.
Mol Syndromol. 2020 Feb;11(1):56-58. doi: 10.1159/000505887. Epub 2020 Feb 1.
Huntington disease (HD) is an autosomal dominant progressive neurodegenerative disorder associated with expanded CAG repeat size in the huntingtin gene and usually presenting with movement disorder, psychiatric symptoms, and cognitive decline. Sleep problems, weight loss, and cachexia are also common. Here, we report a patient presenting with hypothermia in late-stage HD. Although thermoregulatory defects were documented in animal models, this is the first report describing HD with hypothermia in humans.
亨廷顿舞蹈症(HD)是一种常染色体显性进行性神经退行性疾病,与亨廷顿基因中CAG重复序列的扩增有关,通常表现为运动障碍、精神症状和认知能力下降。睡眠问题、体重减轻和恶病质也很常见。在此,我们报告了一名晚期HD患者出现体温过低的情况。尽管在动物模型中已记录到体温调节缺陷,但这是第一份描述人类HD伴体温过低的报告。