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http://hdl.handle.net/11452/25919
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Dublin Core Alanı | Değer | Dil |
---|---|---|
dc.date.accessioned | 2022-04-21T06:13:06Z | - |
dc.date.available | 2022-04-21T06:13:06Z | - |
dc.date.issued | 2003-08 | - |
dc.identifier.citation | Kılıç, S. Ş. vd. (2003). “Esophageal atresia and tracheo-esophageal fistula in a patient with DiGeorge syndrome”. Journal of Pediatric Surgery, 38(8), E21-E23. | en_US |
dc.identifier.issn | 0022-3468 | - |
dc.identifier.uri | https://doi.org/10.1016/S0022-3468(03)00295-1 | - |
dc.identifier.uri | https://www.sciencedirect.com/science/article/pii/S0022346803002951 | - |
dc.identifier.uri | http://hdl.handle.net/11452/25919 | - |
dc.description.abstract | DiGeorge Syndrome (DGS) is a congenital disorder that affects the thymus, parathyroid glands, and heart and brain. Thymus involvement in DGS may vary between absence/hypoplasia of thymus to various forms of reduced T cell function. TBX1 deficiency causes a number of distinct vascular and heart defects, suggesting multiple roles in cardiovascular development, specifically, formation an growth of the pharyngeal arch arteries, growth and septation of the outflow tract of the heart, interventricular septation, and conal alignment. Here the authors describe a case of DGS presenting with severe combined immunodeficiency, esophageal atresia, and tracheoesophageal fistula (TEF). DGS is an important differential diagnosis in TEF. | en_US |
dc.language.iso | en | en_US |
dc.publisher | W B Saunders Co-Elsevier | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Pediatrics | en_US |
dc.subject | Surgery | en_US |
dc.subject | DiGeorge syndrome | en_US |
dc.subject | Esophageal atresia | en_US |
dc.subject | Immunodeficiency | en_US |
dc.subject | Tracheoesophageal fistula | en_US |
dc.subject | 22Q11.2 deletion syndrome | en_US |
dc.subject | Transplantation | en_US |
dc.subject | Diagnosis | en_US |
dc.subject | TBX1 | en_US |
dc.subject | MLCS | en_US |
dc.subject | MLOWN | en_US |
dc.subject.mesh | Abnormalities, multiple | en_US |
dc.subject.mesh | DiGeorge syndrome | en_US |
dc.subject.mesh | Esophageal atresia | en_US |
dc.subject.mesh | Face | en_US |
dc.subject.mesh | Fatal outcome | en_US |
dc.subject.mesh | Heart defects, congenital | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Infant, newborn | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Severe combined immunodeficiency | en_US |
dc.subject.mesh | Tracheoesophageal fistula | en_US |
dc.title | Esophageal atresia and tracheo-esophageal fistula in a patient with DiGeorge syndrome | en_US |
dc.type | Article | en_US |
dc.identifier.wos | 000184649400041 | tr_TR |
dc.identifier.scopus | 2-s2.0-0142248856 | tr_TR |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Çocuk Sağlığı ve Hastalıkları Anabilim Dalı. | tr_TR |
dc.contributor.orcid | 0000-0001-7904-883X | tr_TR |
dc.contributor.orcid | 0000-0001-8571-2581 | tr_TR |
dc.identifier.startpage | E21 | tr_TR |
dc.identifier.endpage | E23 | tr_TR |
dc.identifier.volume | 38 | tr_TR |
dc.identifier.issue | 8 | tr_TR |
dc.relation.journal | Journal of Pediatric Surgery | en_US |
dc.contributor.buuauthor | Kılıç, Sara Şebnem | - |
dc.contributor.buuauthor | Gürpınar, Arif Nuri | - |
dc.contributor.buuauthor | Yakut, Tahsin | - |
dc.contributor.buuauthor | Egeli, Ünal | - |
dc.contributor.buuauthor | Doğruyol, Hasan | - |
dc.contributor.researcherid | AAH-1420-2021 | tr_TR |
dc.subject.wos | Pediatrics | en_US |
dc.subject.wos | Surgery | en_US |
dc.indexed.wos | SCIE | en_US |
dc.indexed.scopus | Scopus | en_US |
dc.wos.quartile | Q2 | en_US |
dc.contributor.scopusid | 34975059200 | tr_TR |
dc.contributor.scopusid | 7004350616 | tr_TR |
dc.contributor.scopusid | 6602802424 | tr_TR |
dc.contributor.scopusid | 55665145000 | tr_TR |
dc.contributor.scopusid | 56624750400 | tr_TR |
dc.subject.scopus | Psychotic Disorders; 22Q11 Deletion Syndrome; Chromosome Loss | en_US |
dc.subject.emtree | Article | en_US |
dc.subject.emtree | Case report | en_US |
dc.subject.emtree | Combined immunodeficiency | en_US |
dc.subject.emtree | Congenital heart malformation | en_US |
dc.subject.emtree | Congenital malformation | en_US |
dc.subject.emtree | DiGeorge syndrome | en_US |
dc.subject.emtree | Esophagus atresia | en_US |
dc.subject.emtree | Face | en_US |
dc.subject.emtree | Fatality | en_US |
dc.subject.emtree | Human | en_US |
dc.subject.emtree | Male | en_US |
dc.subject.emtree | Multiple malformation syndrome | en_US |
dc.subject.emtree | Newborn | en_US |
dc.subject.emtree | Tracheoesophageal fistula | en_US |
Koleksiyonlarda Görünür: | Scopus Web of Science |
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