Saccades in huntington’s disease: Slowing and dysmetria

A. G. Lasker, D. S. Zee, T. C. Hain, S. E. Folstein, H. S. Singer

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Abstract

Eye movements were recorded from 20 mildly affected patients with Huntington's disease (HD) who were divided into two groups, 10 patients with onset of symptoms before age 30 and 10 with onset of symptoms after age 30. In the younger onset group (HD<30), peak saccade velocities were low (<225 deg/sec for 20-deg saccades) in six of the 10 patients, whereas none of the 10 patients in the older onset group (HD>30) had peak saccade velocities lower than 300 deg/sec. Latencies for volitional saccades were greater than normal in the HD>30 group, but were normal for the HD<30 group. The ability to maintain steady fixation in the face of a distracting visual stimulus was decreased, to the same degree, in both groups of HD patients. In addition, 70% of the HD<30 group had an affected father, while 70% of the HD>30 group had an affected mother. These findings suggest that the pathophysiology of the slow saccades, initiation deficit, and excessive distractibility in HD are different.

Original languageEnglish (US)
Pages (from-to)427-431
Number of pages5
JournalNeurology
Volume38
Issue number3
StatePublished - Mar 1988

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ASJC Scopus subject areas

  • Clinical Neurology

Cite this

Lasker, A. G., Zee, D. S., Hain, T. C., Folstein, S. E., & Singer, H. S. (1988). Saccades in huntington’s disease: Slowing and dysmetria. Neurology, 38(3), 427-431.