Vol. 11 (02) pp. 1257-1261 DOI: 10.21474/IJAR01/16375

PROBABLE VOGT-KOYANAGI-HARADA DISEASE: A CASE REPORT

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  • Interneinophthalmology, Hospital of Specialities, University Mohammed V Rabat. Morocco.
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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, Int. J. of Adv. Res., 11 (02), 1257-1261, ISSN 2320-5407. DOI: https://doi.org/10.21474/IJAR01/16375

Corresponding Author

meriem elakhdari
Interne in ophthalmology; hospital of specialities; University Mohammed V Rabat. Morocco
Morocco
Creative Commons Attribution 4.0 This work is licensed under a Creative Commons Attribution 4.0 International License.