{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,8,27]],"date-time":"2025-08-27T15:40:03Z","timestamp":1756309203926,"version":"3.44.0"},"reference-count":12,"publisher":"BMJ","issue":"6","content-domain":{"domain":["bmj.com"],"crossmark-restriction":true},"short-container-title":["BMJ Case Rep"],"accepted":{"date-parts":[[2020,4,27]]},"published-print":{"date-parts":[[2020,6]]},"abstract":"<jats:p>Ebstein anomaly is a congenital heart defect with a low prevalence and high mortality in the early stages of life. In medical literature, there is no reported association between Ebstein anomaly and cri du chat syndrome. Here, we report the case of a full-term newborn with a low weight for his age and who had a prenatal diagnosis of Ebstein anomaly and a postnatal diagnosis of cri du chat syndrome and 20q duplication detected on array CGH. The patient required medical treatment with inotropic support, high-frequency ventilation and nitric oxide, with an adequate response. Surgical intervention was not needed.<\/jats:p>","DOI":"10.1136\/bcr-2019-233766","type":"journal-article","created":{"date-parts":[[2020,6,2]],"date-time":"2020-06-02T05:55:19Z","timestamp":1591077319000},"page":"e233766","update-policy":"https:\/\/doi.org\/10.1136\/crossmarkpolicy","source":"Crossref","is-referenced-by-count":2,"title":["Ebstein anomaly associated with cri du chat (cat\u2019s cry) syndrome and 20q duplication"],"prefix":"10.1136","volume":"13","author":[{"given":"Alberto","family":"Olivella","sequence":"first","affiliation":[{"name":"Universidad del Rosario, Bogot\u00e1, Colombia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-0272-2341","authenticated-orcid":false,"given":"Hernan","family":"Manotas","sequence":"additional","affiliation":[{"name":"Department of Pediatrics, Neonatology, Fundacion Santa Fe de Bogota Hospital Universitario, Bogota, Colombia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-0633-1332","authenticated-orcid":false,"given":"C\u00e9sar","family":"Pay\u00e1n-G\u00f3mez","sequence":"additional","affiliation":[{"name":"Department of Biology, Faculty of Natural Sciences and Mathematics, Universidad del Rosario, Bogota, Colombia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Juan Gabriel","family":"Pi\u00f1eros","sequence":"additional","affiliation":[{"name":"Department of Pediatrics, Neonatology, Fundacion Santa Fe de Bogota Hospital Universitario, Bogota, Colombia"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","published-online":{"date-parts":[[2020,6,1]]},"reference":[{"key":"2025082708261979000_13.6.e233766.1","doi-asserted-by":"crossref","first-page":"211","DOI":"10.1016\/j.pedneo.2016.08.004","article-title":"Ebstein\"s anomaly: genetics, clinical manifestations, and management","volume":"58","author":"Yuan","year":"2017","journal-title":"Pediatr Neonatol"},{"key":"2025082708261979000_13.6.e233766.2","doi-asserted-by":"publisher","DOI":"10.1017\/S1047951114001747"},{"key":"2025082708261979000_13.6.e233766.3","doi-asserted-by":"crossref","first-page":"331","DOI":"10.1053\/j.semtcvs.2017.09.006","article-title":"Neonatal Ebstein anomaly.","volume":"29","author":"Kumar","year":"2017","journal-title":"Semin Thorac Cardiovasc Surg"},{"key":"2025082708261979000_13.6.e233766.4","doi-asserted-by":"crossref","first-page":"e473","DOI":"10.4317\/medoral.15.e473","article-title":"Cri du chat syndrome: a critical review","volume":"15","author":"Rodr\u00edguez-Caballero","year":"2010","journal-title":"Med Oral Patol Oral Cir Bucal"},{"key":"2025082708261979000_13.6.e233766.5","unstructured":"Sweeney S . Cri du chat syndrome: case presentation and review. 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