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Risk factors for accommodative esotropia among hypermetropic children
Eileen E Birch1, Sherry L Fawcett, Sarah E Morale
1Retina Foundation of the Southwest, Dallas, Texas 75231, USA. ebirch@retinafoundation.org
Insights
Family history, poor stereo vision, and hyperopic anisometropia are key risk factors for accommodative esotropia in children. Identifying these can guide early intervention with glasses or therapy.
Area of Science:
- Ophthalmology
- Pediatric Ophthalmology
- Genetics
Background:
- Accommodative esotropia is a common form of childhood strabismus.
- Early identification of risk factors is crucial for timely intervention.
- Hyperopia is a known risk factor, but specific predictive markers are needed.
Purpose of the Study:
- To identify risk factors for developing accommodative esotropia.
- To determine which children with hyperopia may benefit from early spectacle correction.
- To evaluate the role of family history, binocular sensory function, and refractive error in risk assessment.
Main Methods:
- Family history study: 95 children with accommodative esotropia.
- Binocular sensory function study: 41 children with recent-onset intermittent esotropia.
- Hypermetropia study: 345 children with hyperopia (+2.00 D or greater) and no early esotropia.
Main Results:
- 91% of children with accommodative esotropia had an affected relative.
- 41% showed abnormal random-dot stereoacuity.
- Hypermetropic anisometropia increased accommodative esotropia risk 7.8-fold.
Conclusions:
- Positive family history, subnormal stereopsis, and hypermetropic anisometropia are significant risk factors.
- These factors, combined with refractive screening, can identify children needing early intervention.
- Early spectacle correction or preventive therapy can be guided by these risk assessments.
Purpose:
Identification of risk factors for accommodative esotropia may help to determine which children with hyperopia may benefit from early spectacle correction or preventive therapy.
Methods:
Participants in the family history study were 95 consecutive patients, aged 18 to 60 months, with accommodative esotropia. Participants in the binocular sensory function study were a subgroup of 41 children enrolled in the family history study within 1 month of onset, while the esodeviation was still intermittent. Participants in the hypermetropia study were 345 consecutive patients, ages 12 months to 8 years, with refractive error of +2.00 D or greater and no esodeviation before age 12 months.
Results:
In the family history study, 23% of children with accommodative esotropia had an affected first-degree relative, and 91% had at least one affected relative. In the binocular sensory function study, random-dot stereoacuity was abnormal in 41% of children, whereas an abnormal motion VEP, Worth 4-dot, or positive 4-PD base-out prism responses were present in 4% or less of the children. In the hypermetropia study, patients with a mean spherical equivalent of < +3.00 D and significant anisometropia had a 7.8-fold increased risk for accommodative esotropia over nonanisometropic patients.
Conclusions:
A positive family history, subnormal random-dot stereopsis, and hypermetropic anisometropia each pose a significant risk for the development of accommodative esotropia. Assessment of these risk factors in conjunction with refractive screening should help to identify those children who are most likely to benefit from early spectacle correction or preventive treatment.
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