An 11-year-old girl with Joubert syndrome was evaluated for a dim red reflex in her left eye. Fundus examination revealed retinal telangiectasias bilaterally compatible with Coats-like pigmentary retinopathy, a phenomenon not previously reported in Joubert syndrome. Coats-like exudative retinopathy may result in permanent visual loss if left untreated. The exudative retinopathy was controlled after multiple sessions of indirect laser photocoagulation and cryotherapy, with a good visual outcome.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.jaapos.2016.03.018 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!