LAUSR

Vogt–Koyanagi–Harada (VKH) disease is a potentially sight‐threatening condition that affects the pigmented tissues of the body. The disease is diagnosed based on meticulous anterior and posterior segment examination augmented by the use of investigations. But several cases are misdiagnosed as anterior uveitis leading to inadequate management. Such patients have a very grave prognosis and not much can be done at that stage for their benefit. We report such a case which was inadequately managed, eventually leading to irreversible vision loss. We also outline rarely documented findings in a case of late presentation of VKH, namely, iris depigmentation and transillumination defects with ocular hypotony.