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Updated: Jun 13, 2025

Optical Coherence Tomography: Imaging Mouse Retinal Ganglion Cells In Vivo
Published on: September 22, 2017
Late-onset retinal oxalosis in primary hyperoxaluria type 2
Rupak Bhuyan1, Tyler Maggio2, Christie Thomas2
1Department of Ophthalmology and Visual Sciences, University of Iowa Hospitals and Clinics, 200 Hawkins Drive, Iowa City, IA, 52242, USA.
This case highlights severe, late-onset vision loss from retinal oxalosis in primary hyperoxaluria type 2 (PH2). Early genetic testing is crucial for systemic oxalosis patients, as new treatments emerge.
Area of Science:
- Ophthalmology
- Nephrology
- Medical Genetics
Background:
- Primary hyperoxaluria type 2 (PH2) is a rare metabolic disorder.
- Oxalate nephropathy can lead to end-stage kidney disease.
- Systemic oxalate deposition can affect various organs, including the eyes.
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