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Updated: Feb 5, 2026

Eye-Tracking Control to Assess Cognitive Functions in Patients with Amyotrophic Lateral Sclerosis
Published on: October 13, 2016
Abnormal Oculomotor Functions in Amyotrophic Lateral Sclerosis.
Bong Hui Kang1,2, Jae Il Kim2, Young Min Lim1
1Department of Neurology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea.
Amyotrophic lateral sclerosis (ALS) patients show early-stage oculomotor dysfunction, particularly those with bulbar-onset disease. These eye movement abnormalities suggest neurodegeneration beyond motor neurons in ALS.
Area of Science:
- Neuroscience
- Ophthalmology
- Neurology
Background:
- Amyotrophic lateral sclerosis (ALS) is increasingly recognized as affecting extra-motor brain regions, including the cerebellum.
- Oculomotor dysfunction, previously thought to be spared, is now observed in ALS patients.
Purpose of the Study:
- To investigate oculomotor dysfunction in ALS patients.
- To compare eye movement abnormalities between bulbar-onset and spinal-onset ALS patients.
Main Methods:
- An observational study involving 32 ALS patients (10 bulbar-onset, 22 spinal-onset).
- Standardized systemic evaluations using video-oculography were performed.
Main Results:
- Early-stage oculomotor dysfunctions including square wave jerks, saccadic dysmetria, abnormal smooth pursuits, and nystagmus were observed.
- Bulbar-onset ALS patients exhibited significantly more abnormal smooth pursuits and saccadic dysmetria compared to spinal-onset patients (p<0.05).
Conclusions:
- Oculomotor abnormalities may indicate neurodegeneration beyond motor neurons in ALS, particularly in bulbar-onset cases.
- Future longitudinal studies on eye movement abnormalities can offer insights into ALS disease progression and distribution.
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