Cargando…
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...
| Autores principales: | , , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
SMC Media Srl
2018
|
| Materias: | |
| 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 |