Purpose: To report long-term follow-up in a patient with retinal oxalosis from primary hyperoxaluria.
Methods: Retrospective chart review was performed for this patient.
Patients: A 6-year-old girl that presented to our clinic before and after combined kidney/liver transplant.
Results: Optical coherence tomography and fundus findings consistent with oxalate crystal deposition.
Conclusion: Progressive macular changes, including atrophy and fibrosis can occur in crystalline retinopathy, secondary to hyperoxaluria, after combined hepatorenal transplant.
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| http://dx.doi.org/10.1097/ICB.0000000000000272 | DOI Listing |
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