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Higher order aberrations in children with Down syndrome.
Sara J McCullough1, Julie-Anne Little, Kathryn J Saunders
1Vision Science Research Group, School of Biomedical Sciences, University of Ulster, Coleraine, Northern Ireland BT52 1SA. sj.mccullough@ulster.ac.uk
Investigative Ophthalmology & Visual Science
|January 31, 2013
Summary
Children with Down syndrome (DS) have more higher order aberrations (HOAs) and reduced optical quality compared to controls. These subtle differences may impact visual function in DS.
Area of Science:
- Ophthalmology
- Genetics
- Vision Science
Background:
- Down syndrome (DS) is linked to ocular abnormalities and diminished visual function.
- Atypical optical structures, including thinner and steeper corneas and lenses, are reported in DS eyes.
- These optical differences can negatively affect visual acuity.
Purpose of the Study:
- To investigate and compare higher order ocular aberrations (HOAs) in children with DS versus age-matched controls.
- To further understand the impact of ocular structures on visual function in Down syndrome.
Main Methods:
- Shack-Hartmann aberrometry was used to measure HOAs in 44 children with DS and 209 controls (ages 6-16).
- HOAs were analyzed using Zernike polynomials across 3-mm and 5-mm pupils.
- Visual Strehl ratios (VSX) and equivalent defocus values assessed overall optical quality.
Main Results:
- Children with DS exhibited significantly greater total HOAs, third and sixth order aberrations, and coma (P < 0.005).
- Specific Zernike coefficients (Z3(-3), Z3(3), Z0(4)) showed significant differences between groups (P < 0.013).
- DS eyes demonstrated significantly poorer optical quality, as indicated by VSX and equivalent defocus (P < 0.02).
Conclusions:
- Children with DS possess higher HOAs and reduced central optical quality compared to typically developing children.
- While statistically significant, the HOA differences were not considered pathological.
- The observed subtle reduction in optical quality in DS eyes may exacerbate existing visuocortical deficits.
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