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Published on: December 5, 2014
Ocular motor features of alternating hemiplegia of childhood
1Casey Eye Institute, Portland, Oregon, USA.
Insights
Alternating hemiplegia of childhood, a rare neurological disorder, can cause unusual eye movements during episodes. This case highlights repetitive eye abduction jerks during spasms, a potentially unique ocular motor abnormality.
Area of Science:
- Neurology
- Ophthalmology
- Pediatrics
Background:
- Alternating hemiplegia of childhood (AHC) is a rare idiopathic disorder affecting infants and young children.
- It is characterized by recurrent, episodic attacks of hemiplegia or hemiparesis affecting alternating sides of the body.
- The exact pathophysiology of AHC remains largely unknown.
Observation:
- A 14-month-old boy diagnosed with AHC presented with specific ocular motor abnormalities during his episodes.
- During spells, the patient exhibited repetitive jerking movements of eye abduction.
- This occurred in the eye ipsilateral to the affected body side.
Findings:
- The observed repetitive jerks of ipsilateral eye abduction represent a novel finding in the context of AHC.
- This specific ocular motor manifestation has not been previously documented in the literature for this disorder.
- The precise neurobiological mechanism underlying this eye movement abnormality is yet to be determined.
Implications:
- This case suggests that specific ocular motor abnormalities may be a characteristic feature of alternating hemiplegia of childhood.
- Further research into these ocular motor patterns could provide insights into the underlying pathophysiology of AHC.
- Identifying unique clinical signs may aid in earlier diagnosis and understanding of this rare childhood neurological disorder.
Abstract:
A 14-month-old boy with alternating hemiplegia of childhood, an idiopathic disorder of early childhood causing episodic hemibody tonic spasms and hemiplegia, showed repetitive jerks of abduction of the ipsilateral eye during the spells. The mechanism of this ocular motor abnormality is unknown but may be unique to this disorder.
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