Vogt–Koyanagi–Harada Disease, a Rare Entity in Spain: The Challenge of Worldwide Immigration and Globalization

Vogt–Koyanagi–Harada disease is rare, mediated by autoimmune melanocyte inflammation and facilitated by genetic predisposition([1–3]). The main clinical features include uveitis, meningitis, tinnitus and sensorineural deafness, and skin and hair depigmentation. It usually develops in four consecutiv...

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Detalles Bibliográficos
Autores principales: Fernández, Alberto Benavente, Moyano, Sara Pérez, Husein-ElAhmed, Husein, Juárez, Ana María Alfaro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SMC Media Srl 2018
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6346778/
https://www.ncbi.nlm.nih.gov/pubmed/30756049
http://dx.doi.org/10.12890/2018_000886

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6346778/
https://www.ncbi.nlm.nih.gov/pubmed/30756049
http://dx.doi.org/10.12890/2018_000886

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