Slow saccades and other eye movement disorders in spinocerebellar atrophy type 1

@article{Klostermann1997SlowSA,
  title={Slow saccades and other eye movement disorders in spinocerebellar atrophy type 1},
  author={Wolfgang Klostermann and Christine Zuehlke and Wolfgang Heide and Detlef K{\"o}mpf and Karl Wessel},
  journal={Journal of Neurology},
  year={1997},
  volume={244},
  pages={105-111}
}
Abstract In order to study the relation between genotype and phenotype, a detailed study of the course of oculomotor deficits was performed in three patients with autosomal-dominant cerebellar ataxia, subtype spinocerebellar atrophy type 1 (SCA 1) using clinical testing and electrooculography. DNA analysis revealed a CAG repeat expansion of 65 in the SCA 1 gene on chromosome 6p in all patients. A progressive disorder of the saccadic system became obvious, leading to a marked slowing of saccadic… CONTINUE READING
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