PROBABLE VOGT-KOYANAGI-HARADA DISEASE: A CASE REPORT
- Interneinophthalmology, Hospital of Specialities, University Mohammed V Rabat. Morocco.
Abstract
Vogt-Koyanagi-Harada(VKH)diseaseisabilateralgranulomatouspanuveitis affecting young adults, withor without systemic manifestations. The prognosis of VKH disease is generally favorable, however the development of complicationscanleadto blindnessanddeafness.(1)
In this case, we report a 22-year-old man who developed probable Vogt–Koyanagi–Haradadisease without any systemic symptoms, but with several risk factors for poor visual prognosisbeforetreatment,andwhowassuccessfullytreatedwithintensivecorticosteroidtherapy.
Our aim is to describe a clinical case with bilateral serous retinal detachment that presumed asprobableVKHdisease.
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How to Cite This Article
Elakhdari M., Akannour Y., Bardi C., Mrad K., Hassina S., Serghini L., El Hassan A. and Berraho A. (2023); PROBABLE VOGT-KOYANAGI-HARADA DISEASE: A CASE REPORT, International Journal of Advanced Research (IJAR), 11 (02), 1257-1261, ISSN 2320-5407. DOI: https://doi.org/10.21474/IJAR01/16375
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