{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,6,4]],"date-time":"2025-06-04T16:40:07Z","timestamp":1749055207157,"version":"3.41.0"},"reference-count":21,"publisher":"S. Karger AG","issue":"1","license":[{"start":{"date-parts":[[2025,1,21]],"date-time":"2025-01-21T00:00:00Z","timestamp":1737417600000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/karger.com\/pages\/terms-and-conditions"},{"start":{"date-parts":[[2025,1,21]],"date-time":"2025-01-21T00:00:00Z","timestamp":1737417600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/karger.com\/pages\/terms-and-conditions"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Cytogenet Genome Res"],"abstract":"<jats:p>Introduction: Congenital cardiac defects are defined in cases with the deletion of the short arm of chromosome 5 and the duplication of the long arm of chromosome 4. Septal defects and patent ductus arteriosus are among the most common defects reported in the literature. Case Presentation: We reported on a case with a complex congenital cardiac defect, dysmorphic facial features, cat-like cry, hypotonia, hyporeflexia, weak swallowing and sucking, limb anomalies, and bilateral undescended testicles. A chromosomal microarray (CMA) revealed a duplication of chromosome 4q26q35.2 and a deletion of chromosome 5p15.33p14.3, originating from the balanced maternal translocation 46,XX,t(4;5)(q27;pter). Our patient showed clinical characteristics compatible with both deletion of 5p and duplication of 4q. Conclusion: We reported a case with a rare chromosomal rearrangement. Similarities and differences between the cases in the literature are discussed. CMA is important to detect multiple copy number variations and genes may be involved. Studies are needed to investigate the genetic and\/or epigenetic causes resulting in the clinical findings seen in the combination of deletion of chromosome 5p and duplication of chromosome 4q. <\/jats:p>","DOI":"10.1159\/000543591","type":"journal-article","created":{"date-parts":[[2025,1,21]],"date-time":"2025-01-21T17:00:54Z","timestamp":1737478854000},"page":"31-38","source":"Crossref","is-referenced-by-count":1,"title":["Complex Congenital Cardiac Defect Associated with the Combination of 5p Deletion and 4q Duplication in a Newborn: A Case Report"],"prefix":"10.1159","volume":"165","author":[{"given":"\u00dclk\u00fc Nur","family":"K\u0131rman","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ferid","family":"Aliyev","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Merve","family":"So\u011fukp\u0131nar","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Pelin \u00d6zlem","family":"\u015eim\u015fek Kiper","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hayrettin Hakan","family":"Aykan","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hasan Tolga","family":"\u00c7elik","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"127","published-online":{"date-parts":[[2025,1,21]]},"reference":[{"key":"ref1","doi-asserted-by":"publisher","DOI":"10.1186\/s13039-019-0462-0"},{"key":"ref2","doi-asserted-by":"publisher","DOI":"10.1016\/j.ejmg.2010.08.008"},{"key":"ref3","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.a.36396"},{"key":"ref4","doi-asserted-by":"publisher","DOI":"10.1016\/j.ajhg.2010.04.006"},{"key":"ref5","doi-asserted-by":"publisher","DOI":"10.1155\/2016\/5467083"},{"key":"ref6","doi-asserted-by":"publisher","DOI":"10.5507\/bp.2006.016"},{"key":"ref7","doi-asserted-by":"publisher","DOI":"10.1186\/s12884-024-06978-y"},{"key":"ref8","doi-asserted-by":"publisher","DOI":"10.1093\/hmg\/ddt099"},{"key":"ref9","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.10140"},{"key":"ref10","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.a.37005"},{"key":"ref11","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320390412"},{"key":"ref12","doi-asserted-by":"publisher","DOI":"10.1186\/s13039-021-00568-9"},{"key":"ref13","doi-asserted-by":"publisher","DOI":"10.1136\/bcr-2019-233766"},{"key":"ref14","doi-asserted-by":"publisher","DOI":"10.1159\/000506892"},{"key":"ref15","doi-asserted-by":"publisher","DOI":"10.1542\/peds.2005-1012"},{"key":"ref16","doi-asserted-by":"publisher","DOI":"10.1016\/j.ejmg.2011.11.005"},{"key":"ref17","doi-asserted-by":"publisher","DOI":"10.1002\/pd.4782"},{"key":"ref18","doi-asserted-by":"publisher","DOI":"10.1155\/2012\/153405"},{"key":"ref19","doi-asserted-by":"publisher","DOI":"10.1186\/s13039-020-00492-4"},{"key":"ref20","doi-asserted-by":"publisher","DOI":"10.1007\/s12041-014-0318-7"},{"key":"ref21","doi-asserted-by":"publisher","DOI":"10.12998\/wjcc.v10.i30.11031"}],"container-title":["Cytogenetic and Genome Research"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/karger.com\/article-pdf\/doi\/10.1159\/000543591","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/karger.com\/article-pdf\/doi\/10.1159\/000543591","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,6,4]],"date-time":"2025-06-04T16:02:59Z","timestamp":1749052979000},"score":1,"resource":{"primary":{"URL":"https:\/\/karger.com\/article\/doi\/10.1159\/000543591"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2025,1,21]]},"references-count":21,"journal-issue":{"issue":"1","published-online":{"date-parts":[[2025,6,4]]},"published-print":{"date-parts":[[2025,6,4]]}},"URL":"https:\/\/doi.org\/10.1159\/000543591","archive":["Portico"],"relation":{},"ISSN":["1424-8581","1424-859X"],"issn-type":[{"type":"print","value":"1424-8581"},{"type":"electronic","value":"1424-859X"}],"subject":[],"published":{"date-parts":[[2025,1,21]]}}}