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The Double Bubble Sign: Duodenal Atresia and Associated Genetic Etiologies.
Bishop, Juliet C; McCormick, Bridgette; Johnson, Clark T; Miller, Jena; Jelin, Eric; Blakemore, Karin; Jelin, Angie C.
Afiliação
  • Bishop JC; Division of Maternal-Fetal Medicine, Department of Gynecology and Obstetrics, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA, jbisho24@jhmi.edu.
  • McCormick B; Division of Maternal-Fetal Medicine, Department of Gynecology and Obstetrics, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
  • Johnson CT; Division of Maternal-Fetal Medicine, Department of Gynecology and Obstetrics, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
  • Miller J; The Johns Hopkins Center for Fetal Therapy, Baltimore, Maryland, USA.
  • Jelin E; Department of Pediatric Surgery, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
  • Blakemore K; Division of Maternal-Fetal Medicine, Department of Gynecology and Obstetrics, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
  • Jelin AC; Division of Maternal-Fetal Medicine, Department of Gynecology and Obstetrics, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Fetal Diagn Ther ; 47(2): 98-103, 2020.
Article em En | MEDLINE | ID: mdl-31167209
BACKGROUND: The "double bubble" sign is an ultrasonographic finding that commonly represents duodenal atresia and is associated with trisomy 21. OBJECTIVES: We sought to evaluate the positive predictive value of a prenatally identified double bubble sign for duodenal atresia and the genetic etiologies associated with it. METHODS: We examined a retrospective cohort with prenatal double bubble sign between January 1, 2008, and June 30, 2017. Postnatal diagnoses were determined by review of operative reports and additional postnatal evaluation including cytogenetic analysis, molecular analysis, and/or clinical genetic evaluation. RESULTS: All live births at our institution with a prenatal double bubble sign had confirmed duodenal atresia. Additional anatomic anomalies and/or genetic abnormalities were identified in 62% of cases. Out of 21 cases, 6 had trisomy 21. Of the remaining 15 cases, 8 were nonisolated duodenal atresia, 3 of which had a heterotaxy syndrome. In the 7 isolated cases, 1 likely pathogenic chromosomal microdeletion was identified. CONCLUSIONS: Prenatal double bubble sign is a reliable predictor of duodenal atresia. In addition to trisomy 21, heterotaxy may be encountered. ZIC3 mutations as well as microdeletion of 4q22.3 may be underlying genetic etiologies to be considered in the diagnostic evaluation of a prenatal double bubble sign.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ultrassonografia Pré-Natal / Obstrução Duodenal / Atresia Intestinal Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Fetal Diagn Ther Assunto da revista: DIAGNOSTICO POR IMAGEM / OBSTETRICIA / PERINATOLOGIA Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ultrassonografia Pré-Natal / Obstrução Duodenal / Atresia Intestinal Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Fetal Diagn Ther Assunto da revista: DIAGNOSTICO POR IMAGEM / OBSTETRICIA / PERINATOLOGIA Ano de publicação: 2020 Tipo de documento: Article