Goldenhar syndrome with situs inversus totalis

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dc.authorid0000-0001-8142-8794en_US
dc.contributor.authorGörgü, Metin
dc.contributor.authorAslan, Gürcan
dc.contributor.authorErdoğan, Bülent
dc.contributor.authorKaraca, C.
dc.contributor.authorAköz, Tayfun
dc.date.accessioned2024-07-12T21:13:46Z
dc.date.available2024-07-12T21:13:46Z
dc.date.issued1998en_US
dc.departmentFakülteler, Tıp Fakültesien_US
dc.description.abstractGoldenhar syndrome (oculo-auriculovertebral spectrum) is a common disorder with a birth prevalence of about one case per 5600 births. The syndrome has been rKviewed extensively elsewhere 1'2. Hundreds of cases have been reported. We present a case of Goldenhar syndrome with total situs inversus. An affected 15-month-old female is shown in Fig. 1. The father had been operated on for ear anomalies 20 years earlier. Radiographs (Fig. 2) demonstrated vertebral anomalies, scoliosis, and dextrocardia. Ultrasonagraphic examination (Fig. 2) showed a left-sided liver and a right-sided spleen. To our knowledge, situs inversus totalis has not previously been reported with Goldenhar syndrome.en_US
dc.identifier.citationGörgü, M., Aslan, G., Erdoğan, B., Karaca, C. ve Aköz, T. (1998). Goldenhar syndrome with situs inversus totalis. International Journal of Oral & Maxillofacial Surgery. 27(5), s. 404.en_US
dc.identifier.endpage404en_US
dc.identifier.issn0901-5027
dc.identifier.issue5en_US
dc.identifier.scopusqualityQ1en_US
dc.identifier.startpage404en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12415/4562
dc.identifier.volume27en_US
dc.language.isoenen_US
dc.publisherMunksgaarden_US
dc.relation.publicationcategoryUluslararası Hakemli Dergide Makale - Kurum Öğretim Elemanıen_US
dc.rightsCC0 1.0 Universal*
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.rights.urihttp://creativecommons.org/publicdomain/zero/1.0/*
dc.snmzKY04060
dc.titleGoldenhar syndrome with situs inversus totalisen_US
dc.typeArticle
dspace.entity.typePublication

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