ArticleCureus2026
Vogt-Koyanagi-Harada Disease: A Case Report Through Poliosis and Inflammatory Relapses.
Article in Cureus, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Authors and funding
5 authors.
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No grant is acknowledged in the PubMed record.
Abstract
Vogt-Koyanagi-Harada (VKH) disease is a rare autoimmune stromal choroiditis affecting melanocyte-rich tissues and typically presenting with bilateral ocular inflammation associated with neurological, auditory, or integumentary manifestations. Early diagnosis is essential because prompt initiation of intensive immunosuppressive therapy is associated with improved long-term outcomes. An 18-year-old Hispanic man presented in September 2022 with a one-week history of bilateral visual loss and ocular redness. He had experienced a first episode of anterior uveitis in June 2022 and subsequently developed marked depigmentation of the hair, eyebrows, beard, and eyelashes beginning in July 2022. Ophthalmic examination and multimodal imaging demonstrated bilateral granulomatous panuveitis with active stromal choroiditis. Extensive infectious and inflammatory investigations were negative, while
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