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- W4366993863 abstract "Aim: To report a rare case with Sturge-Weber Syndrome associated with central serous retinopathy. SWS is a rare sporadic genetic disease and diagnosis is primarily done by evaluating history, the presence of port-wine stain, and characteristic features on brain radio imaging. As no denitive treatment is available yet, patients are being treated by medical and surgical interventions for symptoms as well as for associated complications. Material And Methods: 18-year-old male presented with blurred vision and was found to have elevated intraocular pressure (IOP) and glaucomatous disc damage in the left eye. He also displayed capillary malformation (port-wine stain) on the same side of the face. IOP got reduced after prescribing a topical anti-glaucoma drug. This case exhibits a very rare occurrence of Sturge-Weber syndrome affecting the left side of the face associated with ipsilateral central serous retinopathy. The patient responded Result: well to the topical beta-blocker in the subsequent follow-up when the IOP was found to be well controlled. Central serous retinopathy also got reduced in 1 month with no changes in BCVA. Sturge-Weber syndrome is a Conclusion: rare phacomatosis that may present with central serous retinopathy" @default.
- W4366993863 created "2023-04-27" @default.
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- W4366993863 date "2023-03-15" @default.
- W4366993863 modified "2023-09-30" @default.
- W4366993863 title "STURGE-WEBER SYNDROME ASSOCIATED WITH CENTRAL SEROUS RETINOPATHY: A RARE CASE SCENARIO" @default.
- W4366993863 doi "https://doi.org/10.36106/gjra/9012174" @default.
- W4366993863 hasPublicationYear "2023" @default.
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