{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,25]],"date-time":"2026-09-25T15:44:46Z","timestamp":1790351086157,"version":"4.1.0"},"reference-count":20,"publisher":"Wiley","license":[{"start":{"date-parts":[[2014,1,1]],"date-time":"2014-01-01T00:00:00Z","timestamp":1388534400000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/3.0\/"}],"funder":[{"DOI":"10.13039\/100007833","name":"Hamad Medical Corporation","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100007833","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Case Reports in Pediatrics"],"published-print":{"date-parts":[[2014]]},"abstract":"<jats:p>Congenital diaphragmatic hernia is a common developmental anomaly encountered by paediatric surgeons. It is known to be associated with extradiaphragmatic malformations, which include cardiac, renal, genital, and chromosomal abnormalities. Herein, we report a newborn born with concurrent congenital diaphragmatic hernia, Meckel\u2019s diverticulum, and heterotopic pancreatic tissue. This is the first case report of such a triad with description of possible mechanisms of the development.<\/jats:p>","DOI":"10.1155\/2014\/725945","type":"journal-article","created":{"date-parts":[[2014,4,3]],"date-time":"2014-04-03T17:08:28Z","timestamp":1396544908000},"page":"1-3","source":"Crossref","is-referenced-by-count":2,"title":["A Triad of Congenital Diaphragmatic Hernia, Meckel\u2019s Diverticulum, and Heterotopic Pancreas"],"prefix":"10.1155","volume":"2014","author":[{"given":"Parkash","family":"Mandhan","sequence":"first","affiliation":[{"name":"Department of Pediatric Surgery, Hamad General Hospital, Hamad Medical Corporation, P.O. 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