{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,11,21]],"date-time":"2023-11-21T12:43:53Z","timestamp":1700570633052},"reference-count":25,"publisher":"Wiley","issue":"8","license":[{"start":{"date-parts":[[2007,4,27]],"date-time":"2007-04-27T00:00:00Z","timestamp":1177632000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Birth Defects Research"],"published-print":{"date-parts":[[2007,8]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p><jats:bold>BACKGROUND:<\/jats:bold> An association between the triple\u2010X syndrome (47,XXX) and gastrointestinal malformations is extremely rare. Most 47,XXX patients present with a normal phenotype, but genitourinary malformations have been described. <jats:bold>CASE:<\/jats:bold> We report a case of a child with 47,XXX and duodenal atresia. Antenatal ultrasound scan showed a dilated fetal stomach and upper part of the duodenum (double bubble phenomenon) at 31 weeks of gestation in a 31\u2010year\u2010old woman with polyhydramnion. The amniotic fluid karyotype showed 47,XXX. After a scheduled delivery, duodenal atresia was confirmed and treated with duodeno\u2010duodenostomy. <jats:bold>CONCLUSIONS:<\/jats:bold> The possible association of gastrointestinal and genitourinary tract anomalies requires a detailed postnatal clinical investigation and ultrasonographic examination of the abdomen, retroperitoneum, and pelvis on all triple\u2010X syndrome patients. Birth Defects Research (Part A) 2007. \u00a9 2007 Wiley\u2010Liss, Inc.<\/jats:p>","DOI":"10.1002\/bdra.20371","type":"journal-article","created":{"date-parts":[[2007,4,27]],"date-time":"2007-04-27T21:49:59Z","timestamp":1177710599000},"page":"612-613","source":"Crossref","is-referenced-by-count":5,"title":["Duodenal atresia in an infant with triple\u2010X syndrome: A new associated malformation in 47,XXX"],"prefix":"10.1002","volume":"79","author":[{"given":"Udo","family":"Rolle","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Barbara","family":"Linse","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Simone","family":"Glasow","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Klaus Rainer","family":"Sandig","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Thomas","family":"Richter","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Holger","family":"Till","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2007,8,3]]},"reference":[{"key":"e_1_2_4_2_1","doi-asserted-by":"publisher","DOI":"10.1055\/s-2008-1026874"},{"key":"e_1_2_4_3_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1399-0004.1983.tb00443.x"},{"key":"e_1_2_4_4_1","first-page":"123","article-title":"Un cas de syndrometriplo X avec malformations multiples","volume":"9","author":"Gilgenkrantz S","year":"1966","journal-title":"Ann Genet"},{"key":"e_1_2_4_5_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0165-4608(03)00100-6"},{"key":"e_1_2_4_6_1","first-page":"A151","article-title":"47,XXX with mullerian agenesis","volume":"65","author":"Guze C","year":"1999","journal-title":"Am J Hum Genet"},{"key":"e_1_2_4_7_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.a.20393"},{"key":"e_1_2_4_8_1","doi-asserted-by":"publisher","DOI":"10.1007\/s100249900090"},{"key":"e_1_2_4_9_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320330220"},{"key":"e_1_2_4_10_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320360114"},{"key":"e_1_2_4_11_1","first-page":"63","volume-title":"Population Cytogenetics. Studies in Humans","author":"Hook EB","year":"1979"},{"key":"e_1_2_4_12_1","first-page":"78","volume-title":"Smith's recognizable patterns of human malformation","author":"Jones KL","year":"1997"},{"key":"e_1_2_4_13_1","doi-asserted-by":"publisher","DOI":"10.1016\/0020-7292(95)02395-S"},{"key":"e_1_2_4_14_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1479-828X.1980.tb00110.x"},{"key":"e_1_2_4_15_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320450619"},{"key":"e_1_2_4_16_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.10391"},{"key":"e_1_2_4_17_1","doi-asserted-by":"crossref","first-page":"619","DOI":"10.1542\/peds.82.4.619","article-title":"47,XXX. What is the prognosis?","volume":"82","author":"Linden MG","year":"1988","journal-title":"Pediatrics"},{"key":"e_1_2_4_18_1","first-page":"26","article-title":"Un cas d'aplasie utero\u2010vaginale avec polykystose renale et mosaique XX\u2010XXX","volume":"20","author":"Linquette M","year":"1968","journal-title":"Bull Fed Soc Gynecol Obstet"},{"key":"e_1_2_4_19_1","unstructured":"MartinRA.2002.Fryns syndrome without a diaphragmatic hernia. A case report and review of this uncommon presentation. David W. 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