Article
Eye-tracking-aided characterization of saccades and antisaccades in SYNE1 ataxia patients: a pilot study.
BMC neuroscience - 1 Feb 2021
Szpisjak Laszlo, Szaraz Gabor, Salamon Andras, Nemeth Viola L, Szepfalusi Noemi, Veres Gabor, Kincses Balint, Maroti Zoltan, Kalmar Tibor, Rydzanicz Malgorzata, Ploski Rafal, Klivenyi Peter, Zadori Denes
Abstract excerpt
BACKGROUND: SYNE1 ataxia is an autosomal recessive hereditary condition, the main characteristic features of which are gait and limb ataxia and cerebellar dysarthria. Reports have revealed that the clinical phenotype of SYNE1 ataxia is more complex than the first published cases with pure cerebellar signs indicated. The aim of this study was to characterize eye movement alterations in the first diagnosed...
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