Department of Neurology H2-237, Academic Medical Centre, University of Amsterdam, PO Box 22660, 1100 DD Amsterdam, The Netherlands.
J Neurol Neurosurg Psychiatry. 2010 Feb;81(2):228-30. doi: 10.1136/jnnp.2008.170902.
Huntington disease (HD) is a neurodegenerative disorder associated with an expanded CAG trinucleotide repeat length in the huntingtin gene. 'Intermediate alleles' with 27 to 35 CAG repeats generally do not cause HD but are unstable upon germ-line transmission. Insights in CAG repeat mosaicism and enhanced trinucleotide expansion in postmitotic neurons indicate that in the intermediate range, other factors than the CAG repeat length in diagnostic tests have to be considered. Here, we report two patients with mild, late onset HD and an intermediate repeat allele. The authors anticipate that intermediate repeats can cause late-onset HD due to disease modifiers and may be more common than previously stated.
亨廷顿病(HD)是一种神经退行性疾病,与亨廷顿基因中 CAG 三核苷酸重复长度的扩展有关。具有 27 到 35 个 CAG 重复的“中间等位基因”通常不会导致 HD,但在种系传播时不稳定。对 CAG 重复镶嵌和有丝分裂后神经元中三核苷酸扩展的深入了解表明,在中间范围内,除了诊断测试中的 CAG 重复长度外,还必须考虑其他因素。在这里,我们报告了两名患有轻度、迟发性 HD 和中间重复等位基因的患者。作者预计,由于疾病修饰因子,中间重复可能会导致迟发性 HD,并且可能比之前所述更为常见。