2023-03-082023-03-082016-02-16Dorum, B. A. vd. (2016). "Serpentine-like syndrome associated with encephalocele". Clinical Dysmorphology, 25(3), 110-112.0962-88271473-5717https://doi.org/10.1097/MCD.0000000000000122https://journals.lww.com/clindysmorphol/Fulltext/2016/07000/Serpentine_like_syndrome_associated_with.5.aspxhttp://hdl.handle.net/11452/31429Congenital 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.eninfo:eu-repo/semantics/closedAccessGenetics & heredityCongenital intrathoracic stomachBrachioesophagusRachischisisHerniaEchocardiographyEncephaloceleFemaleGenetic association studiesHumansInfant, newbornMagnetic resonance imagingPhenotypePrenatal diagnosisRadiography, thoracicSyndromeSerpentine-like syndrome associated with encephaloceleArticle0003786138000052-s2.0-8496019396711011225326950236Genetics & heredityHiatus Hernia; Stomach Volvulus; HernioplastyAntibiotic agentAdultAntibiotic therapyApgar scoreArticleArtificial ventilationAspiration pneumoniaBirth weightCase reportCongenital diaphragm herniaCongenital malformationCystic lymphangiomaDisease associationEchocardiographyEchographyEncephaloceleEnteric feedingEsophagus malformationFemaleFetus echographyGestational ageHead circumferenceHumanHydramniosJejunostomyMagnetic resonance angiographyNotochordNuclear magnetic resonance imagingPatent ductus arteriosusPriority journalSerpentine like syndromeSplit notochord malformationTachypneaThorax radiographyTotal parenteral nutritionVertebra malformationEncephaloceleGenetic association studyGeneticsNewbornPhenotypePrenatal diagnosisSyndrome