WordNet

present at birth but not necessarily hereditary; acquired during fetal development (同)inborn, innate
an abnormal condition in which a normal opening or tube in the body (as the urethra) is closed or absent
in or relating to the duodenum; "duodenal ulcer"

PrepTutorEJDIC

(病気・身体的欠陥など)生まれつきの,先天的な
十二指腸の

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1. 腸管閉鎖症intestinal atresia [show details]
…include: Duodenal atresia – Vomiting may or may not be bilious. Approximately 30 percent of newborns with duodenal atresia have Down syndrome. In infants without Down syndrome, other congenital malformations …
2. 先天性消化管閉鎖症（食道、十二指腸・小腸・大腸、直腸・肛門など）の出生前診断prenatal diagnosis of esophageal gastrointestinal and anorectal atresia [show details]
…most frequent cause of duodenal atresia, occurring in up to 30 percent of cases . Congenital heart disease – Twenty to 30 percent of fetuses with duodenal atresia have congenital heart disease . VACTERL …
3. 輪状膵annular pancreas [show details]
…pancreas has been associated with maternal polyhydramnios and congenital abnormalities such as Down syndrome, esophageal and duodenal atresia, imperforate anus, and Meckel diverticulum . The pancreas …
4. 胸腔内気道の先天異常および気管食道瘻congenital anomalies of the intrathoracic airways and tracheoesophageal fistula [show details]
… association with a spectrum of congenital anomalies described as TACRD (tracheal agenesis/atresia, complex congenital cardiac abnormalities, radial ray defects, and duodenal atresia) . In case series of fetuses …
5. ダウン症候群：出生前スクリーニングの概要down syndrome overview of prenatal screening [show details]
…time to evaluate the fetus for congenital anomalies associated with Down syndrome. These fetuses are at increased risk for congenital heart defects and duodenal atresia. The widespread implementation …

English Journal

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XL-EDA-ID Presenting with Congenital Duodenal Atresia and Perforations.

Mitani Y1, Wada T2, Matsuda Y1, Sakai S3, Yachie A1.
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Prenatal Diagnosis of Recurrent Distal 1q21.1 Duplication in Three Fetuses With Ultrasound Anomalies.

Ji X1, Pan Q2, Wang Y1, Wu Y1, Zhou J1, Liu A1, Qiao F1, Ma D1, Hu P1, Xu Z1.
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PMID 30177949