Mahale, Ajit and Ullal, Sonali and Fernandes, Merwyn and *, Mithun Shekar (2013) A rare case of Vogt–Koyanagi–Harada (VKH) disease. Transworld Medical Journal, 1 (2). pp. 144-146. ISSN 23472790
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Abstract
Vogt-Koyanagi-Harada (VKH) disease is a rare idiopathic chronic granulomatous inflammatory disorder. It has ophthalmic, neurological and cutaneous manifestations. Clinical picture is dependent on the stage of presentation. We report a case of VKH syndrome presenting with rapid deterioration of visual acquity and vitiligo.
Item Type: | Article |
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Uncontrolled Keywords: | chronic granulomatous disease |
Subjects: | Medicine > KMC Mangalore > Radio Diagnosis and Imaging |
Depositing User: | KMCMLR User |
Date Deposited: | 14 Feb 2014 06:57 |
Last Modified: | 14 Feb 2014 06:57 |
URI: | http://eprints.manipal.edu/id/eprint/138846 |
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