A CASE REPORT OF VOGTS KOYANAGI-HARADA SYNDROME
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Abstract
Introduction: Vogt-Koyanagi-Harada syndrome (VKH) is a rare multi-systemic disease that affects tissues containing melanin, such as the eye, inner ear, meninges, and skin. It is characterized by chronic bilateral panuveitis associated with auditory, neurological, and cutaneous manifestations. Material and Methodology : A 19 years old female presented to the out patient department of the ophthalmology department of Maharani Laxmi Bai Medical College, Jhansi with the following complaints for Drooping of upper eyelid in left eye since childhood and Retraction of left upper eyelid on jaw movement .
How to Cite This Article
Silky Saraf (2026); A CASE REPORT OF VOGTS KOYANAGI-HARADA SYNDROME, International Journal of Advanced Research (IJAR), 14 (08), 1086-1091, ISSN 2320-5407.
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