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http://hdl.handle.net/11452/31429
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DC Field | Value | Language |
---|---|---|
dc.date.accessioned | 2023-03-08T10:32:11Z | - |
dc.date.available | 2023-03-08T10:32:11Z | - |
dc.date.issued | 2016-02-16 | - |
dc.identifier.citation | Dorum, B. A. vd. (2016). "Serpentine-like syndrome associated with encephalocele". Clinical Dysmorphology, 25(3), 110-112. | en_US |
dc.identifier.issn | 0962-8827 | - |
dc.identifier.issn | 1473-5717 | - |
dc.identifier.uri | https://doi.org/10.1097/MCD.0000000000000122 | - |
dc.identifier.uri | https://journals.lww.com/clindysmorphol/Fulltext/2016/07000/Serpentine_like_syndrome_associated_with.5.aspx | - |
dc.identifier.uri | http://hdl.handle.net/11452/31429 | - |
dc.description.abstract | Congenital short oesophagus and with intrathoracic development of the stomach is a rare developmental anomaly of the gastrointestinal system. Knowledge regarding its aetiology and management is limited. We report a case in which, in addition to short oesophagus and intrathoracic stomach, an encephalocele was identified during the antenatal period. After the postpartum examination, encephalocele, split notochord malformation, midline localized liver and congenital short oesophagus were confirmed. The report of this case adds to the body of knowledge on this rare condition. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Lippincott Williams & Wilkins | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Genetics & heredity | en_US |
dc.subject | Congenital intrathoracic stomach | en_US |
dc.subject | Brachioesophagus | en_US |
dc.subject | Rachischisis | en_US |
dc.subject | Hernia | en_US |
dc.subject.mesh | Echocardiography | en_US |
dc.subject.mesh | Encephalocele | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Genetic association studies | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Infant, newborn | en_US |
dc.subject.mesh | Magnetic resonance imaging | en_US |
dc.subject.mesh | Phenotype | en_US |
dc.subject.mesh | Prenatal diagnosis | en_US |
dc.subject.mesh | Radiography, thoracic | en_US |
dc.subject.mesh | Syndrome | en_US |
dc.title | Serpentine-like syndrome associated with encephalocele | en_US |
dc.type | Article | en_US |
dc.identifier.wos | 000378613800005 | tr_TR |
dc.identifier.scopus | 2-s2.0-84960193967 | tr_TR |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Neonatoloji Anabilim Dalı. | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Çocuk Sağlığı ve Hastalıkları Anabilim Dalı. | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Çocuk Radyolojisi Anabilim Dalı. | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Çocuk Cerrahisi Anabilim Dalı. | tr_TR |
dc.contributor.orcid | 0000-0002-2823-8454 | tr_TR |
dc.identifier.startpage | 110 | tr_TR |
dc.identifier.endpage | 112 | tr_TR |
dc.identifier.volume | 25 | tr_TR |
dc.identifier.issue | 3 | tr_TR |
dc.relation.journal | Clinical Dysmorphology | en_US |
dc.contributor.buuauthor | Dorum, Bayram Ali | - |
dc.contributor.buuauthor | Korkmaz, Serpil | - |
dc.contributor.buuauthor | Özkan, Hilal | - |
dc.contributor.buuauthor | Köksal, Nilgün | - |
dc.contributor.buuauthor | Bağcı, Onur | - |
dc.contributor.buuauthor | Yazıcı, Zeynep | - |
dc.contributor.buuauthor | Gürpınar, Arif Nuri | - |
dc.contributor.researcherid | AAI-2303-2021 | tr_TR |
dc.contributor.researcherid | AAG-8393-2021 | tr_TR |
dc.contributor.researcherid | A-5375-2017 | tr_TR |
dc.identifier.pubmed | 26950236 | tr_TR |
dc.subject.wos | Genetics & heredity | en_US |
dc.indexed.wos | SCIE | en_US |
dc.indexed.scopus | Scopus | en_US |
dc.indexed.pubmed | PubMed | en_US |
dc.wos.quartile | Q4 | en_US |
dc.contributor.scopusid | 37661266800 | tr_TR |
dc.contributor.scopusid | 57159045100 | tr_TR |
dc.contributor.scopusid | 16679325400 | tr_TR |
dc.contributor.scopusid | 7003323615 | tr_TR |
dc.contributor.scopusid | 20733563300 | tr_TR |
dc.contributor.scopusid | 6701668723 | tr_TR |
dc.contributor.scopusid | 7004350616 | tr_TR |
dc.subject.scopus | Hiatus Hernia; Stomach Volvulus; Hernioplasty | en_US |
dc.subject.emtree | Antibiotic agent | en_US |
dc.subject.emtree | Adult | en_US |
dc.subject.emtree | Antibiotic therapy | en_US |
dc.subject.emtree | Apgar score | en_US |
dc.subject.emtree | Article | en_US |
dc.subject.emtree | Artificial ventilation | en_US |
dc.subject.emtree | Aspiration pneumonia | en_US |
dc.subject.emtree | Birth weight | en_US |
dc.subject.emtree | Case report | en_US |
dc.subject.emtree | Congenital diaphragm hernia | en_US |
dc.subject.emtree | Congenital malformation | en_US |
dc.subject.emtree | Cystic lymphangioma | en_US |
dc.subject.emtree | Disease association | en_US |
dc.subject.emtree | Echocardiography | en_US |
dc.subject.emtree | Echography | en_US |
dc.subject.emtree | Encephalocele | en_US |
dc.subject.emtree | Enteric feeding | en_US |
dc.subject.emtree | Esophagus malformation | en_US |
dc.subject.emtree | Female | en_US |
dc.subject.emtree | Fetus echography | en_US |
dc.subject.emtree | Gestational age | en_US |
dc.subject.emtree | Head circumference | en_US |
dc.subject.emtree | Human | en_US |
dc.subject.emtree | Hydramnios | en_US |
dc.subject.emtree | Jejunostomy | en_US |
dc.subject.emtree | Magnetic resonance angiography | en_US |
dc.subject.emtree | Notochord | en_US |
dc.subject.emtree | Nuclear magnetic resonance imaging | en_US |
dc.subject.emtree | Patent ductus arteriosus | en_US |
dc.subject.emtree | Priority journal | en_US |
dc.subject.emtree | Serpentine like syndrome | en_US |
dc.subject.emtree | Split notochord malformation | en_US |
dc.subject.emtree | Tachypnea | en_US |
dc.subject.emtree | Thorax radiography | en_US |
dc.subject.emtree | Total parenteral nutrition | en_US |
dc.subject.emtree | Vertebra malformation | en_US |
dc.subject.emtree | Encephalocele | en_US |
dc.subject.emtree | Genetic association study | en_US |
dc.subject.emtree | Genetics | en_US |
dc.subject.emtree | Newborn | en_US |
dc.subject.emtree | Phenotype | en_US |
dc.subject.emtree | Prenatal diagnosis | en_US |
dc.subject.emtree | Syndrome | en_US |
Appears in Collections: | Scopus Web of Science |
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