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dc.contributor.authorÇağlar, İsmail Çağatay
dc.contributor.authorBatur, Muhammed
dc.contributor.authorSeven, Erbil
dc.contributor.authorTekin, Serek
dc.contributor.authorYaşar, Tekin
dc.date.accessioned2019-05-13T09:03:06Z
dc.date.available2019-05-13T09:03:06Z
dc.date.issued2017
dc.identifier.citationÇağlar, Ç., Batur, M., Seven, E., Tekin, S., Yaşar, T. (2017). Congenital hypothyroidism in Axen-feld-Rieger syndrome. Eastern Journal of Medicine, 22(4), 208-210.en_US
dc.identifier.issn1301-0883
dc.identifier.urihttps://doi.org/10.5505/ejm.2017.07269
dc.identifier.urihttps://hdl.handle.net/11491/1404
dc.description.abstractAxenfeld-Rieger syndrome (ARS) manifests varying degrees of anterior segment dysgenesis and carries a risk of resistant glaucoma. It can affect ocular and extraocular structures derived from the neural crest. A small part of the thyroid gland originates from the neural crest, and defects in thyroid origination can result in thyroid agenesis. Thyroid agenesis is a cause of congenital hypothyroidism. We have presented clinical features the first case of ARS associated with congenital hypothyroidism. © 2017, Yuzuncu Yil Universitesi Tip Fakultesi. All rights reserved.en_US
dc.language.isoeng
dc.publisherYüzüncü Yıl Üniversitesi Tıp Fakültesien_US
dc.relation.isversionof10.5505/ejm.2017.07269en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAnterior Segment Dysgenesisen_US
dc.subjectAxenfeld-Rieger Syndromeen_US
dc.subjectCongenital Hypothyroidismen_US
dc.subjectNeural Cresten_US
dc.subjectThyroid Agenesisen_US
dc.titleCongenital hypothyroidism in Axenfeld-Rieger syndromeen_US
dc.typearticleen_US
dc.relation.journalEastern Journal of Medicineen_US
dc.departmentHitit Üniversitesi, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümüen_US
dc.authorid0000-0003-4391-2571en_US
dc.identifier.volume22en_US
dc.identifier.issue4en_US
dc.identifier.startpage208en_US
dc.identifier.endpage210en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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