Bürk K, Zühlke C, König I R, Ziegler A, Schwinger E, Globas C, Dichgans J, Hellenbroich Y
Department of Neurology, University of Tübingen, Germany.
Neurology. 2004 Jan 27;62(2):327-9. doi: 10.1212/01.wnl.0000103293.63340.c1.
The authors report a German family with autosomal dominant cerebellar ataxia tightly linked to the spinocerebellar ataxia type 5 (SCA5) locus (multipoint lod score 5.76). The phenotype is characterized by a purely cerebellar syndrome with a downbeat nystagmus occurring prior to the development of other features. Imaging studies demonstrated cortical cerebellar atrophy. Progression is slow even in patients with a disease onset during the second decade. The age at onset varies from 15 to 50 years.
作者报告了一个德国家庭,其常染色体显性遗传性小脑共济失调与5型脊髓小脑共济失调(SCA5)基因座紧密连锁(多点连锁值为5.76)。该表型的特征是单纯的小脑综合征,在出现其他症状之前就有下跳性眼球震颤。影像学研究显示小脑皮质萎缩。即使是在第二个十年发病的患者,病情进展也很缓慢。发病年龄在15至50岁之间。