{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,18]],"date-time":"2026-08-18T02:08:05Z","timestamp":1787018885115,"version":"build-2736575974"},"reference-count":12,"publisher":"SAGE Publications","issue":"4","license":[{"start":{"date-parts":[[2014,4,24]],"date-time":"2014-04-24T00:00:00Z","timestamp":1398297600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"content-domain":{"domain":["journals.sagepub.com"],"crossmark-restriction":true},"short-container-title":["J Child Neurol"],"published-print":{"date-parts":[[2015,3]]},"abstract":"<jats:p>A preterm neonate presenting with respiratory distress after birth was found to have a clival encephalocele, which is a variant of a basal encephalocele, and hypoplasia of the cerebellum. Genetic studies revealed a small deletion of the long arm of chromosome 5: 5q15 deletion. We report a rare variant of a basal encephalocele with a cerebellar malformation and 5q15 deletion.<\/jats:p>","DOI":"10.1177\/0883073814530504","type":"journal-article","created":{"date-parts":[[2014,4,24]],"date-time":"2014-04-24T21:08:20Z","timestamp":1398373700000},"page":"505-508","update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":5,"title":["Clival Encephalocele and 5q15 Deletion:"],"prefix":"10.1177","volume":"30","author":[{"given":"Surasak","family":"Puvabanditsin","sequence":"first","affiliation":[{"name":"Department of Pediatrics, Rutgers Robert Wood Johnson Medical School, New Brunswick, NJ, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Imran","family":"Malik","sequence":"additional","affiliation":[{"name":"Department of Pediatrics, Rutgers Robert Wood Johnson Medical School, New Brunswick, NJ, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Eugene","family":"Garrow","sequence":"additional","affiliation":[{"name":"Department of Surgery, SUNY Downstate Medical Center, Brooklyn, New York, NY, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lissa","family":"Francois","sequence":"additional","affiliation":[{"name":"Department of Obstetrics and Genecology, Rutgers RWJ Medical School, New Brunswick, NJ, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Rajeev","family":"Mehta","sequence":"additional","affiliation":[{"name":"Department of Pediatrics, Rutgers Robert Wood Johnson Medical School, New Brunswick, NJ, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"179","published-online":{"date-parts":[[2014,4,24]]},"reference":[{"key":"bibr1-0883073814530504","doi-asserted-by":"publisher","DOI":"10.1097\/00005537-200210000-00018"},{"key":"bibr2-0883073814530504","doi-asserted-by":"publisher","DOI":"10.1055\/s-0030-1261261"},{"key":"bibr3-0883073814530504","doi-asserted-by":"publisher","DOI":"10.4103\/2152-7806.90034"},{"key":"bibr4-0883073814530504","doi-asserted-by":"publisher","DOI":"10.3171\/jns.2000.93.3.0513"},{"key":"bibr5-0883073814530504","first-page":"112","volume":"13","author":"Zamann SMQ","year":"2009","journal-title":"Pan Arab J Neurosurg"},{"key":"bibr6-0883073814530504","doi-asserted-by":"publisher","DOI":"10.4103\/2152-7806.106260"},{"key":"bibr7-0883073814530504","doi-asserted-by":"publisher","DOI":"10.3171\/jns.1972.36.2.0201"},{"key":"bibr8-0883073814530504","doi-asserted-by":"publisher","DOI":"10.1177\/014556130608500706"},{"key":"bibr9-0883073814530504","doi-asserted-by":"publisher","DOI":"10.1542\/peds.103.1.e12"},{"key":"bibr10-0883073814530504","first-page":"186","volume":"19","author":"Kalkan G","year":"2013","journal-title":"Hong Kong Med J"},{"key":"bibr11-0883073814530504","first-page":"154","volume":"35","author":"Hashemi B","year":"2010","journal-title":"IJMS"},{"key":"bibr12-0883073814530504","unstructured":"Brenner G, Chung HYB, Shannon P, Toi A, Shaffer L, Chitayat D. The first reported case of the DRAGON gene deletion in human. A case with a de-novo interstitial deletion of chromosome 5q15-21.1. Available at: www.ashg.org\/2009meeting\/abstracts\/fulltext\/f20465.htm."}],"container-title":["Journal of Child Neurology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/journals.sagepub.com\/doi\/pdf\/10.1177\/0883073814530504","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/journals.sagepub.com\/doi\/full-xml\/10.1177\/0883073814530504","content-type":"application\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/journals.sagepub.com\/doi\/pdf\/10.1177\/0883073814530504","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,4,29]],"date-time":"2026-04-29T20:36:44Z","timestamp":1777495004000},"score":1,"resource":{"primary":{"URL":"https:\/\/journals.sagepub.com\/doi\/10.1177\/0883073814530504"}},"subtitle":["A Case Report"],"short-title":[],"issued":{"date-parts":[[2014,4,24]]},"references-count":12,"journal-issue":{"issue":"4","published-print":{"date-parts":[[2015,3]]}},"alternative-id":["10.1177\/0883073814530504"],"URL":"https:\/\/doi.org\/10.1177\/0883073814530504","relation":{},"ISSN":["0883-0738","1708-8283"],"issn-type":[{"value":"0883-0738","type":"print"},{"value":"1708-8283","type":"electronic"}],"subject":[],"published":{"date-parts":[[2014,4,24]]}}}