Ocular findings in patients with waardenburg syndrome
dc.contributor.author | Önder, Halil Ibrahim | |
dc.contributor.author | Tunç, Murat | |
dc.contributor.author | Yüksel, Harun | |
dc.contributor.author | Sılan, Fatma | |
dc.contributor.author | Kaya, Murat | |
dc.date.accessioned | 2025-01-27T19:04:04Z | |
dc.date.available | 2025-01-27T19:04:04Z | |
dc.date.issued | 2013 | |
dc.department | Çanakkale Onsekiz Mart Üniversitesi | |
dc.description.abstract | Waardenburg Syndrome (WS) is a heterogenous group of auditory-pigmentary syndromes.WS is characterized by the association of pigmentation abnormalities, including depigmented patches of the skin and hair, vivid blue eyes or heterochromia irides, and sensorineural hearing loss. Hearing loss and other phenotypic expression is highly variable. WS can be seen with a frequency of 1/20000 - 1/42000 in different populations. © 2013 Düzce Medical Journal. | |
dc.identifier.endpage | 63 | |
dc.identifier.issn | 1307-671X | |
dc.identifier.issue | 3 | |
dc.identifier.scopus | 2-s2.0-84940227316 | |
dc.identifier.scopusquality | Q3 | |
dc.identifier.startpage | 60 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12428/13790 | |
dc.identifier.volume | 15 | |
dc.indekslendigikaynak | Scopus | |
dc.language.iso | en | |
dc.publisher | Duzce University Medical School | |
dc.relation.ispartof | Duzce Medical Journal | |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | |
dc.rights | info:eu-repo/semantics/closedAccess | |
dc.snmz | KA_Scopus_20250125 | |
dc.subject | Deafness; Iris heterochromia; Waardenburg syndrome | |
dc.title | Ocular findings in patients with waardenburg syndrome | |
dc.title.alternative | Waardenburg sendromlu hastalarda göz bulgulari | |
dc.type | Review Article |