Vogt-Koyanagi-Harada Syndrome in a 10 Years Old Child

Sufi, AR; Zargar, S and Singh, T (2011) Vogt-Koyanagi-Harada Syndrome in a 10 Years Old Child. Online Journal of Health and Allied Sciences, 10 (2). ISSN 0972-5997

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Abstract

The Vogt-Koyanagi-Harada (VKH) syndrome is a rare systemic disorder of uveitis, dysacousia, vitiligo, premature graying of the hair, eyebrows and eyelashes, and meningoencephalitis. Although frequently unrecognised,VKH may affect children. We report a case of a 10 year old girl who presented with headache and dimness of vision and was diagnosed as papillitis on the basis of bilateral disc edema. However over the course of time developed skin changes (poliosis, vitiligo over lower back) and depigmented patches in inferior fundus suggesting diagnosis of VKH disease. Thus the diagnosis is difficult in the absence of extraocular manifestations. In such cases the diagnosis is based on clinical evolution of the disease.

EPrint Type:Article
Uncontrolled Keywords:Vogt-Koyanagi-Harada Syndrome; Poliosis; Vitiligo; Uveitis
Subjects:Eye Diseases > Uveal Diseases > Uveitis
-Journal Repositories > Online Journal of Health and Allied Sciences
ID Code:3825
Deposited By:Dr Srinivas Kakkilaya
Deposited On:06 August 2012

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