Bishop Juliet C, McCormick Bridgette, Johnson Clark T, Miller Jena, Jelin Eric, Blakemore Karin, Jelin Angie C
Division of Maternal-Fetal Medicine, Department of Gynecology and Obstetrics, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA,
Division of Maternal-Fetal Medicine, Department of Gynecology and Obstetrics, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Fetal Diagn Ther. 2020;47(2):98-103. doi: 10.1159/000500471. Epub 2019 Jun 5.
The "double bubble" sign is an ultrasonographic finding that commonly represents duodenal atresia and is associated with trisomy 21.
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.
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.
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.
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.
“双泡征”是一种超声检查结果,通常提示十二指肠闭锁,且与21-三体综合征相关。
我们旨在评估产前发现的双泡征对十二指肠闭锁的阳性预测价值及其相关的遗传病因。
我们对2008年1月1日至2017年6月30日期间有产前双泡征的回顾性队列进行了研究。通过查阅手术报告及产后的其他评估,包括细胞遗传学分析、分子分析和/或临床遗传学评估来确定产后诊断。
我们机构所有产前有双泡征的活产婴儿均确诊为十二指肠闭锁。62%的病例还发现了其他解剖异常和/或遗传异常。在21例病例中,6例为21-三体综合征。其余15例中,8例为非孤立性十二指肠闭锁,其中3例伴有内脏异位综合征。在7例孤立病例中,发现1例可能致病的染色体微缺失。
产前双泡征是十二指肠闭锁的可靠预测指标。除21-三体综合征外,还可能出现内脏异位。ZIC3突变以及4q22.3微缺失可能是产前双泡征诊断评估中需考虑的潜在遗传病因。