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dc.contributor.authorŞen, Ahmet
dc.contributor.authorÇalapoğlu, Ahmet Salih
dc.contributor.authorŞen, Habibe
dc.date.accessioned2020-12-19T20:51:36Z
dc.date.available2020-12-19T20:51:36Z
dc.date.issued2015
dc.identifier.citationŞen, A, Çalapoğlu, A.S., Şen, H. (2015). Anesthetic management of cornelia de lange syndrome: a case report. Erciyes Medical Journal, 37(1), 43-44.
dc.identifier.issn2149-2247
dc.identifier.issn2149-2549
dc.identifier.urihttps://app.trdizin.gov.tr/makale/TVRjMU1USXlNZz09
dc.identifier.urihttps://hdl.handle.net/11436/6081
dc.description.abstractCornelia de Lange syndrome (CdLS) is described as a congenital disease characterized by delayed growth, mental-motor retardation, typical face appearance, thick eyebrows meeting at the midline, micrognathia, thin lips, micromelia, dental problems, and malformations in the systems such as cardiac, gastrointestinal, genitourinary, and musculoskeletal systems. It is rarely seen, with a reported incidence of 1 in 10,000 to 40,000. It is generally sporadic, but can also be dominant and recessive (1). Problems such as difficult intubation, gastroesophageal reflux, aspiration, and hyperthermia make the airway safety more difficult in general anesthesia practices (2). We aimed to present our anesthesia management experience with a patient having CdLS who was operated because of undescended testis and circumcision after taking the consent of his family.en_US
dc.language.isoengen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectGenel ve Dahili Tıpen_US
dc.titleAnesthetic management of cornelia de lange syndrome: a case reporten_US
dc.typeletteren_US
dc.contributor.departmentRTEÜ, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümüen_US
dc.identifier.volume37en_US
dc.identifier.issue1en_US
dc.identifier.startpage43en_US
dc.identifier.endpage44en_US
dc.ri.editoaen_US
dc.relation.journalErciyes Medical Journalen_US
dc.relation.publicationcategoryDiğeren_US


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