Vogt-Koyanagi-Harada Disease in an Adolescent Boy
dc.contributor.author | Bilgic, Ozlem | |
dc.contributor.author | Gunduz, Abuzer | |
dc.contributor.author | Kaya, Kismet | |
dc.date.accessioned | 2020-03-26T18:58:46Z | |
dc.date.available | 2020-03-26T18:58:46Z | |
dc.date.issued | 2014 | |
dc.department | Selçuk Üniversitesi | en_US |
dc.description.abstract | Vogt-Koyanagi-Harada (VKH) disease is a rare multiorgan disorder that affects the melanocytes of the eyes, skin, inner ear, and meninges. It is more common in women and in patients 30 to 50 years of age; it is rarely seen in children. We report a 14-year-old boy who meets the criteria for complete VKH disease. | en_US |
dc.identifier.doi | 10.1111/pde.12163 | en_US |
dc.identifier.endpage | 101 | en_US |
dc.identifier.issn | 0736-8046 | en_US |
dc.identifier.issn | 1525-1470 | en_US |
dc.identifier.issue | 1 | en_US |
dc.identifier.pmid | 23869531 | en_US |
dc.identifier.scopusquality | Q2 | en_US |
dc.identifier.startpage | 99 | en_US |
dc.identifier.uri | https://dx.doi.org/10.1111/pde.12163 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12395/31279 | |
dc.identifier.volume | 31 | en_US |
dc.identifier.wos | WOS:000330951800033 | en_US |
dc.identifier.wosquality | Q3 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.language.iso | en | en_US |
dc.publisher | WILEY-BLACKWELL | en_US |
dc.relation.ispartof | PEDIATRIC DERMATOLOGY | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.selcuk | 20240510_oaig | en_US |
dc.title | Vogt-Koyanagi-Harada Disease in an Adolescent Boy | en_US |
dc.type | Article | en_US |