Alport syndrome is characterized by type IV collagen network disruptions leading to renal, auditory, and ocular manifestations. This case report details a 24-year-old man with Alport syndrome who developed a rhegmatogenous retinal detachment following macular hole repair. The patient underwent a successful vitrectomy and internal limiting membrane peel for macular hole repair but returned with vision loss due to retinal detachment five weeks later, which necessitated a combined scleral buckle and vitrectomy. This is the first case describing rhegmatogenous retinal detachment post-macular hole repair in Alport syndrome. .
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.3928/23258160-20240208-01 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!