Latanaprost treatment of the heterochromia in a patient with acquired Horner syndrome

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dc.contributor.authorOksuz, H.
dc.contributor.authorTamer, C.
dc.contributor.authorMelek, I. M.
dc.date.accessioned2024-09-18T20:26:48Z
dc.date.available2024-09-18T20:26:48Z
dc.date.issued2006
dc.departmentHatay Mustafa Kemal Üniversitesien_US
dc.description.abstractHorner syndrome results from either congenital or acquired causes of sympathetic denervation. Heterochromia, a clinical feature of congenital Horner syndrome, is quite rare in acquired Horner syndrome, especially after the age of two. There were only a few cases reported previously. We reported a 24-year-old man who was diagnosed up on pharmacological tests and clinical findings as acquired Horner syndrome with heterochromia. The main complaint of the patient was hypochromia on the affected side, which was obviously improved after 19 months of latanoprost treatment.en_US
dc.identifier.doi10.1080/01658100600981253
dc.identifier.endpage131en_US
dc.identifier.issn0165-8107
dc.identifier.issue5en_US
dc.identifier.scopus2-s2.0-33750553826en_US
dc.identifier.scopusqualityQ3en_US
dc.identifier.startpage129en_US
dc.identifier.urihttps://doi.org/10.1080/01658100600981253
dc.identifier.urihttps://hdl.handle.net/20.500.12483/10542
dc.identifier.volume30en_US
dc.identifier.wosWOS:000241725100005en_US
dc.identifier.wosqualityQ4en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.publisherTaylor & Francis Incen_US
dc.relation.ispartofNeuro-Ophthalmologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectHorner syndromeen_US
dc.subjectheterochromiaen_US
dc.subjectlatanoprosten_US
dc.titleLatanaprost treatment of the heterochromia in a patient with acquired Horner syndromeen_US
dc.typeArticleen_US

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