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Spectral domain optical coherence tomography finding in posterior microphthalmos
Mukesh Kumar1, Taraprasad Das, Siddharth Kesarwani
1L V Prasad Eye Institute, Bhubaneswar, Orissa, India. Mukesh.Opt@gmail.com
Clinical & Experimental Optometry
|July 27, 2012
Summary
This case report details a young boy with posterior microphthalmos, a condition causing decreased vision. Optical coherence tomography revealed specific retinal layer folds, offering new insights into this rare eye disorder.
Area of Science:
- Ophthalmology
- Retinal Imaging
- Pediatric Ophthalmology
Background:
- Posterior microphthalmos is a rare congenital condition characterized by a small eye with a normal anterior segment and a relatively long axial length.
- Decreased vision in pediatric patients can be caused by various refractive errors and structural abnormalities of the eye.
Observation:
- An eight-year-old boy presented with significantly reduced visual acuity (6/60) in both eyes, corrected with high plus spheres.
- Ocular examination revealed normal anterior segments but fundus findings and spectral domain optical coherence tomography (SD-OCT) were indicative of posterior microphthalmos.
- SD-OCT imaging demonstrated an elevated foveal contour and a fold within the outer plexiform layer, sparing the external limiting membrane, photoreceptors, and retinal pigment epithelium.
Findings:
- The spectral domain optical coherence tomography findings in this case provide detailed imaging of the specific retinal layers affected by the fold in posterior microphthalmos.
- This is the first reported case of posterior microphthalmos with optical coherence tomography imaging that precisely identifies the retinal layers involved in the observed fold.
Implications:
- This detailed imaging contributes to a better understanding of the structural changes associated with posterior microphthalmos.
- The findings highlight the utility of SD-OCT in diagnosing and characterizing rare pediatric retinal conditions.
- Further research into the pathogenesis and management of posterior microphthalmos may benefit from such detailed case reports.
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