Vogt-Koyanagi-Harada disease and bilateral simultaneous Adie’s pupil
Journal Title: BOHR International Journal of Current Research in Optometry and Ophthalmology - Year 2024, Vol 3, Issue 1
Abstract
Vogt-Koyanagi-Harada (VKH) syndrome is an uncommon autoimmune inflammatory malady commonly accompanied by neurological, auditory, and integumentary signs. We report a case of a teenage girl who complained of persistently decreased vision for the last 15 days. There was no systemic association. After 2 weeks, the patient developed tonic pupils. The pupil showed a tonic response to a 0.125% pilocarpine eye drop. Upon examinations, the patient was diagnosed with Vogt-Koyanagi-Harada disease and bilateral Adie’s pupil, which is a rare conditions associated with VKH disease. Early treatment is crucial for preserving vision
Authors and Affiliations
Most. Sanjida Akter Syeed Mehbub Ul Kadir Razia Shultana Sarwat Rahman Md. ZahedurRahman Rajendra Prakash Maurya
Keywords
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- EP ID EP750686
- DOI 10.54646/bijcroo.2024.38
- Views 23
- Downloads 0
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Vogt-Koyanagi-Harada (VKH) syndrome is an uncommon autoimmune inflammatory malady commonly accompanied by neurological, auditory, and integumentary signs. We report a case of a teenage girl who complained of persistently...
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