Vogt-Koyanagi-Harada (VKH) syndrome is a rare systemic disease involving various melanocyte-containing organs. Bilateral panuveitis associated with cutaneous, neurologic, and auditory abnormalities are manifestations of this inflammatory granulomatous disorder.
Today I added a new case of VKH with typical ICG findings. You can see photos directly by clickingon the title of this post.
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