Eye movement abnormalities correlate with genotype in autosomal dominant cerebellar ataxia type I.

doi:10.1002/ana.410430306

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Article

Eye movement abnormalities correlate with genotype in autosomal dominant cerebellar ataxia type I.

Annals of neurology - 1 Mar 1998

Rivaud-Pechoux S, Dürr A, Gaymard B, Cancel G, Ploner C J, Agid Y, Brice A, Pierrot-Deseilligny C

Abstract excerpt

We compared horizontal eye movements (visually guided saccades, antisaccades, and smooth pursuit) in control subjects (n = 14) and patients with three forms of autosomal dominant cerebellar ataxias type I: spinocerebellar ataxias 1 and 2 (SCA1, n = 11; SCA2, n = 10) and SCA3/Machado-Joseph diseas...

Topics

Adolescent
Adult
Aged
Cerebellar Ataxia
Eye Movements
Female
Fixation, Ocular
Genes, Dominant
Genotype
Humans
Male
Middle Aged
Nystagmus, Physiologic
Pursuit, Smooth
Repetitive Sequences, Nucleic Acid
Saccades

Source

Open in PubMed

Identifiers

PMID: 9506545
DOI: 10.1002/ana.410430306

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-9506545-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

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