Vestibulo-ocular reflex abnormality in Vogt-Koyanagi-Harada syndrome.

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Vogt-koyanagi-harada Syndrome

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Vogt-Koyanagi-Harada Syndrome

97 Vogt-Koyanagi-Harada syndrome is generally a rare multisystemic autoimmune disorder involving with pigmented structures, such as the eye, meninges, inner ear and skin. The syndrome typically presents as an episode of bilateral panuveitis after prodromal symptoms similar to aseptic meningitis. Auditory disturbances include tinnitus, hearing loss and vertigo. We report the case of a 74-year-ol...

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Vogt-Koyanagi-Harada syndrome is an uncommon multisystem inflammatory disorder characterized by panuveitis with serous retinal detachment and is often associated with neurologic and cutaneous manifestations including headache, hearing loss, vitiligo, and poliosis. The case of a 62-year-old female with diabetes mellitus and a history of primary open angle glaucoma (POAG) in both eyes, operated o...

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ژورنال

عنوان ژورنال: British Journal of Ophthalmology

سال: 1994

ISSN: 0007-1161

DOI: 10.1136/bjo.78.12.912