A case of unilateral and spontaneously resolving posterior uveitis with overlapping features of Vogt–Koyanagi–Harada disease and Acute Posterior Multifocal Placoid Pigment Epitheliopathy

INTRODUCTION: VKH disease is a chronic, bilateral, granulomatous panuveitis with potential involvement of neurological, auditory and integumentary systems. On the other hand, APMPPE is believed to be an immune-driven chorioretinal vascular disease characterized by multifocal, flat, grey-white placoi...

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Detalles Bibliográficos
Autores principales: Li, Bo, Bentham, Ricarda J., Gonder, John R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2016
Materias:
Case Study
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5009056/
https://www.ncbi.nlm.nih.gov/pubmed/27652046
http://dx.doi.org/10.1186/s40064-016-3132-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5009056/
https://www.ncbi.nlm.nih.gov/pubmed/27652046
http://dx.doi.org/10.1186/s40064-016-3132-2

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