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Related Experiment Video

Updated: Jun 19, 2026

In vivo Structural Assessments of Ocular Disease in Rodent Models using Optical Coherence Tomography
07:44

In vivo Structural Assessments of Ocular Disease in Rodent Models using Optical Coherence Tomography

Published on: July 24, 2020

Ocular Microstructural Alterations in Children With Spina Bifida: An Optical Coherence Tomography Study.

Gamze Ucan Gunduz1, Sema Nizam Tekcan1, Duygu Erdem1

  • 1The Departments of Ophthalmology and.

Journal of Pediatric Ophthalmology and Strabismus
|June 18, 2026
PubMed
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Children with spina bifida show retinal and choroidal changes detectable by optical coherence tomography. These may indicate impaired macular development and are linked to shorter axial length.

Area of Science:

  • Ophthalmology
  • Pediatric Ophthalmology
  • Neuro-ophthalmology

Background:

  • Spina bifida is a complex congenital condition impacting neurological development.
  • Ocular complications in spina bifida are not fully understood.
  • Optical coherence tomography (OCT) allows detailed imaging of retinal and optic nerve head structures.

Purpose of the Study:

  • To investigate microstructural differences in the retina, choroid, and optic nerve head in children with spina bifida compared to healthy controls.
  • To utilize optical coherence tomography (OCT) for detailed ocular tissue analysis.

Main Methods:

  • A cross-sectional study included 38 children with spina bifida and 32 controls, matched for age and sex.
  • Comprehensive ophthalmological examinations were performed.

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Last Updated: Jun 19, 2026

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  • Optical coherence tomography (OCT) was used to image the macula, choroid, and peripapillary retinal nerve fiber layer.
  • Main Results:

    • Children with spina bifida had significantly shorter axial lengths and higher prevalence of hyperopia.
    • While central macular thickness was similar, significant retinal layer differences were observed: thicker outer nuclear layer and thinner inner nuclear and outer plexiform layers.
    • Subfoveal and nasal choroidal thickness were greater in the spina bifida group, but this difference diminished when controlling for axial length.

    Conclusions:

    • Children with spina bifida exhibit retinal and choroidal alterations detectable by OCT.
    • Retinal changes may suggest impaired macular development associated with spina bifida.
    • Choroidal thickness variations appear related to axial length differences in this population.