A rare case of Vogt–Koyanagi–Harada (VKH) disease

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
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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