dc.creatorCuevas M.
dc.creatorde-la-Torre, Alejandra
dc.creatorCórdoba A.
dc.date.accessioned2020-05-25T23:57:40Z
dc.date.accessioned2022-09-22T14:32:42Z
dc.date.available2020-05-25T23:57:40Z
dc.date.available2022-09-22T14:32:42Z
dc.date.created2020-05-25T23:57:40Z
dc.identifier9273948
dc.identifierhttps://repository.urosario.edu.co/handle/10336/22717
dc.identifierhttps://doi.org/10.1080/09273948.2017.1320411
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3439856
dc.description.abstractPurpose: 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. ©, © Taylor and Francis Group, LLC.
dc.languageeng
dc.publisherTaylor and Francis Ltd
dc.relationOcular Immunology and Inflammation, ISSN:9273948, Vol.26, No.7 (2018); pp. 1101-1106
dc.relationhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85019707641&doi=10.1080%2f09273948.2017.1320411&partnerID=40&md5=006a9f59c57db046fdb6b370caf7af91
dc.relation1106
dc.relationNo. 7
dc.relation1101
dc.relationOcular Immunology and Inflammation
dc.relationVol. 26
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rightsAbierto (Texto Completo)
dc.sourceinstname:Universidad del Rosario
dc.sourcereponame:Repositorio Institucional EdocUR
dc.titleBilateral Iris Depigmentation and Ocular Hypotony as End-Stage Manifestations of Untreated Vogt–Koyanagi–Harada Disease
dc.typearticle


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