Alterações encontradas na angiografia por tomografia de coerência óptica (OCT-A) em
            pacientes com síndrome de Alport

Trancoso, Flávio Gusmão; Gallon, Laisa; Bomfim, Maria Luiza de Azevedo; Silva, Antônio Fábio Miguel da; Cade, Fabiano; Zanetti, Fernando Roberte

doi:10.5935/0004-2749.20200088

Cited by 3 publications

(1 citation statement)

References 3 publications

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“…Alport syndrome shows choroidal thickening and significant inner retinal changes. Cogan syndrome is characterized by retinal vasculitis without any subretinal changes [72,73].…”

Section: Alport and Cogan Syndromesmentioning

confidence: 99%

Vogt-Koyanagi-Harada Disease: Current Diagnosis and Management

Goyal,

Shah,

Anantharaman

et al. 2024

Uveitis - Basics, Diagnosis, and Treatment

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Vogt-Koyanagi-Harada (VKH) disease is a rare granulomatous inflammatory disease that affects pigmented structures, such as eye, inner ear, meninges, skin, and hair. This disease is mainly a T1 lymphocyte-mediated aggression to melanocytes. The availability of new investigational methods has improved our knowledge of the pathogenesis, clinical approach, diagnosis, and management of VKH disease. The disease has an acute onset of bilateral blurred vision with hyperemia in the absence of prior ocular trauma or any previous intraocular surgery. The chronic phase comprises of ocular and integumentary system pigmentary changes. Ocular findings may be accompanied by meningismus, hearing impairment, and skin lesions in a variable proportion of patients. Prompt diagnosis with early, aggressive, and long-term treatment of high-dose corticosteroids ensures good visual outcomes. The aim of this chapter is to present the clinicopathology, classification, recent imaging, investigations, and management of VKH disease.

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“…Alport syndrome shows choroidal thickening and significant inner retinal changes. Cogan syndrome is characterized by retinal vasculitis without any subretinal changes [72,73].…”

Section: Alport and Cogan Syndromesmentioning

confidence: 99%