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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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| Publicat a: | Eur J Case Rep Intern Med |
|---|---|
| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
SMC Media Srl
2018
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6346778/ https://ncbi.nlm.nih.gov/pubmed/30756049 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12890/2018_000886 |
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