Rebecca, Murtaza Sameen Junejo, Fahad Feroz Shaikh, Nazir Ashraf Laghari.
Vogt - koyanagi harada syndrome in a pakistani female.
Pak J Ophthalmol Jan ;36(4):23-4.

Vogt-Koyanagi-Harada syndrome is a rare multiorgan inflammatory disorder characterized by bilateral uveitis with serous retinal detachment and is often associated headache, hearing loss, vitiligo, and poliosis. Here we present a case of 37 years old female who presented with chronic photophobia, redness and progressive decreased vision in both eyes for 5 years along with cutaneous and hearing symptoms. On Ocular examination her best-corrected visual acuity was 6/60 OD and perception of light OS, while the intraocular pressure was 16 mm Hg OD and 18 mm Hg OS, measured with Goldmann applanation tonometer. The slit-lamp examination of right anterior segment showed diffuse Keratic precipitates along with diffuse iris atrophy and seclusion pupillae (360 degree). On detailed examination she found to be a case of VKH syndrome. This case is presented to familiarize ophthalmologists and health care professionals about its findings and complications that are usually found in such patients.

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