{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,9,18]],"date-time":"2025-09-18T02:16:49Z","timestamp":1758161809068,"version":"3.44.0"},"reference-count":47,"publisher":"Mathematical Modelling and Numerical Simulation with Applications","issue":"03","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Pediatr Genet"],"published-print":{"date-parts":[[2024,9]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Although 40 years have passed since the first case of DiGeorge's syndrome was described, and the knowledge about this disorder has steadily increased since that time, 22q11.2 deletion syndrome (DS) remains a challenging diagnosis because its clinical presentation varies widely. We describe an infant with 22q11.2 DS who presented with annular pancreas, anorectal malformation, Morgagni-type congenital diaphragmatic hernia, and ventricular septal defect. This constellation of anomalies has never been described in DiGeorge's syndrome. Here, we provide a case presentation and a thorough review of the literature.<\/jats:p>","DOI":"10.1055\/s-0042-1750748","type":"journal-article","created":{"date-parts":[[2022,8,2]],"date-time":"2022-08-02T18:50:15Z","timestamp":1659466215000},"page":"237-244","source":"Crossref","is-referenced-by-count":0,"title":["Multiple Intestinal Anomalies in a Newborn with 22q11.2 Microdeletion Syndrome: A Case Report and Literature Review"],"prefix":"10.53391","volume":"13","author":[{"given":"Bedour","family":"Jafar","sequence":"additional","affiliation":[{"name":"Department of Pediatrics, University of South Alabama, Mobile, Alabama, United States"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hanna","family":"Alemayehu","sequence":"additional","affiliation":[{"name":"Division of Pediatric Surgery, Department of Surgery, University of South Alabama, Mobile, Alabama, United States"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ramachandra","family":"Bhat","sequence":"additional","affiliation":[{"name":"Division of Neonatology, Department of Pediatrics, Louisiana State University Health Science Center, Shreveport, Louisiana, United States"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-2835-7023","authenticated-orcid":false,"given":"Michael","family":"Zayek","sequence":"additional","affiliation":[{"name":"Division of Neonatology, Department of Pediatrics, University of South Alabama, Mobile, Alabama, United States"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"31409","published-online":{"date-parts":[[2022,8,2]]},"reference":[{"issue":"10","key":"ref1","doi-asserted-by":"crossref","first-page":"2203","DOI":"10.1002\/ajmg.a.40494","article-title":"22q and two: 22q11.2 deletion syndrome and coexisting conditions","volume":"176","author":"J L 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