False median cleft: a rare facial anomaly

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dc.authorid0000-0001-8142-8794en_US
dc.contributor.authorAkan, Mithat
dc.contributor.authorYıldırım, Serkan
dc.contributor.authorAvcı, Gülden
dc.contributor.authorAköz, Tayfun
dc.date.accessioned2024-07-12T21:01:47Z
dc.date.available2024-07-12T21:01:47Z
dc.date.issued2001en_US
dc.departmentFakülteler, Tıp Fakültesien_US
dc.description.abstractA false median or pseudomedian cleft lip may be considered an extreme variety of bilateral complete cleft lip from an embryological standpoint. 1 A false median cleft lip is usually associated with holoprosencephaly, hypotelorism, or hypertelorism, and is rarely an isolated defect. A 5-day-old male infant was referred by a pediatrician to our department for evaluation of facial cleft. The child’s delivery was normal, after full-term gestation. The infant’s birthweight was 2,800 g. His mother had had an uneventful pregnancy during which no drugs had been taken. Family history was unremarkable.en_US
dc.identifier.citationAkan, M., Yıldırım, S., Avcı, G. ve Aköz, T. (2001). False median cleft: a rare facial anomaly. Annals of Plastic Surgery. 46(3), s. 350.en_US
dc.identifier.endpage350en_US
dc.identifier.issn1536-3708
dc.identifier.issue3en_US
dc.identifier.scopusqualityQ2en_US
dc.identifier.startpage350en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12415/3533
dc.identifier.volume16en_US
dc.language.isoenen_US
dc.publisherWolters Kluwer Healthen_US
dc.relation.ispartofAnnals of Plastic Surgeryen_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.snmzKY00276
dc.titleFalse median cleft: a rare facial anomalyen_US
dc.typeArticle
dspace.entity.typePublication

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