Abstract
Purpose: To describe severe bilateral iris depigmentation and persistent ocular hypotony as end-stage manifestations of untreated Vogt–Koyanagi–Harada disease. Methods: We present the clinical findings and diagnostic studies performed for three patients with bilateral iris depigmentation. Results: Vogt–Koyanagi–Harada disease in late recurrent stage was diagnosed in three patients with bilateral severe iris depigmentation and persistent ocular hypotony. Conclusions: Early diagnosis and treatment of inflammation are crucial factors in the clinical outcome of Vogt–Koyanagi–Harada disease. When left undiagnosed and untreated from early stages, severe iris depigmentation and ocular hypotony, uncommon manifestations of this disease, can develop.
| Translated title of the contribution | Despigmentación bilateral del iris e hipotonía ocular como manifestaciones en fase terminal de la enfermedad de Vogt-Koyanagi-Harada no tratada. |
|---|---|
| Original language | English (US) |
| Article number | PMID: 28548582 |
| Pages (from-to) | 1-6 |
| Number of pages | 6 |
| Journal | Ocular Immunology and Inflammation |
| Early online date | Mar 26 2017 |
| DOIs | |
| State | Published - May 26 2017 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
All Science Journal Classification (ASJC) codes
- Immunology and Allergy
- Ophthalmology
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