{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,28]],"date-time":"2026-10-28T22:42:50Z","timestamp":1793227370011,"version":"4.5.0"},"reference-count":8,"publisher":"BMJ","issue":"5","content-domain":{"domain":["bmj.com"],"crossmark-restriction":true},"short-container-title":["BMJ Case Rep"],"accepted":{"date-parts":[[2019,4,19]]},"published-print":{"date-parts":[[2019,5]]},"abstract":"<jats:p>Congenital unilateral renal agenesis is a relatively frequent condition at birth diagnosed mostly incidentally. Despite the excellent prognosis, unilateral renal agenesis is associated with an increased risk of other structural abnormalities, including genital malformations. The authors present two cases of asymptomatic adolescents with known congenital unilateral renal agenesis and associated genital malformations solely diagnosed during puberty\u2014a man with Zinner syndrome and a female with Mayer-Rokitansky-K\u00fcster-Hauser syndrome.<\/jats:p>","DOI":"10.1136\/bcr-2018-229034","type":"journal-article","created":{"date-parts":[[2019,5,7]],"date-time":"2019-05-07T12:27:32Z","timestamp":1557232052000},"page":"e229034","update-policy":"https:\/\/doi.org\/10.1136\/crossmarkpolicy","source":"Crossref","is-referenced-by-count":10,"title":["Zinner and Mayer-Rokitansky-K\u00fcster-Hauser syndromes: when unilateral renal agenesis meets genital anomalies"],"prefix":"10.1136","volume":"12","author":[{"given":"Filipa","family":"Briosa","sequence":"first","affiliation":[{"name":"Department of Paediatrics, Hospital Beatriz Angelo, Loures, Portugal"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Rita","family":"Valsassina","sequence":"additional","affiliation":[{"name":"Department of Paediatrics, Hospital Beatriz Angelo, Loures, Portugal"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Catarina","family":"Mira","sequence":"additional","affiliation":[{"name":"Department of Radiology, Hospital Beatriz Angelo, Loures, Portugal"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ana","family":"Zagalo","sequence":"additional","affiliation":[{"name":"Department of Paediatrics, Hospital Beatriz Angelo, Loures, Portugal"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"239","published-online":{"date-parts":[[2019,5,6]]},"reference":[{"key":"2025082702220290000_12.5.e229034.1","first-page":"195","article-title":"Unilateral renal agenesis and uterine anomalies: how and when can we make this diagnosis?","volume":"26","author":"Gaspar","year":"2017","journal-title":"Nascer e Crescer \u2013 Birth and Growth Medical Journal"},{"key":"2025082702220290000_12.5.e229034.2","first-page":"57","article-title":"Association of unilateral renal agenesis and genital anomalies","volume":"3","author":"Barakat","year":"2002","journal-title":"Case Rep Clin Pract Rev"},{"key":"2025082702220290000_12.5.e229034.3","doi-asserted-by":"crossref","unstructured":"Ozcan T . Renal agenesis: Prenatal diagnosis. Post TW, ed. UpToDate. Waltham, MA: UpToDate Inc. http:\/\/www.uptodate.com (Accessed on 17 Oct 2018).","DOI":"10.1097\/01.COT.0000512180.05121.bb"},{"key":"2025082702220290000_12.5.e229034.4","doi-asserted-by":"crossref","first-page":"444","DOI":"10.4103\/0970-1591.70592","article-title":"Zinner syndrome: A unique triad of mesonephric duct abnormalities as an unusual cause of urinary symptoms in late adolescence","volume":"26","author":"Ghonge","year":"2010","journal-title":"Indian J Urol"},{"key":"2025082702220290000_12.5.e229034.5","doi-asserted-by":"crossref","first-page":"313","DOI":"10.1016\/j.radcr.2016.04.002","article-title":"Zinner syndrome-a rare developmental anomaly of the mesonephric duct diagnosed on magnetic resonance imaging","volume":"11","author":"Mehra","year":"2016","journal-title":"Radiol Case Rep"},{"key":"2025082702220290000_12.5.e229034.6","doi-asserted-by":"publisher","DOI":"10.1148\/radiol.13130211"},{"key":"2025082702220290000_12.5.e229034.7","doi-asserted-by":"crossref","first-page":"93","DOI":"10.1111\/j.1744-4667.2012.00097.x","article-title":"Mayer-Rokitansky-K\u00fcster-Hauser syndrome: diagnosis and management","volume":"14","author":"Valappil","year":"2012","journal-title":"The Obstetrician & Gynaecologist"},{"key":"2025082702220290000_12.5.e229034.8","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1155\/2013\/628717","article-title":"Mayer-rokitansky-kuster-hauser syndrome: embryology, genetics and clinical and surgical treatment","volume":"2013","author":"Pizzo","year":"2013","journal-title":"ISRN Obstet Gynecol"}],"container-title":["BMJ Case Reports"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/syndication.highwire.org\/content\/doi\/10.1136\/bcr-2018-229034","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,8,27]],"date-time":"2025-08-27T09:22:07Z","timestamp":1756286527000},"score":1,"resource":{"primary":{"URL":"https:\/\/casereports.bmj.com\/lookup\/doi\/10.1136\/bcr-2018-229034"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2019,5]]},"references-count":8,"journal-issue":{"issue":"5","published-online":{"date-parts":[[2019,5,6]]},"published-print":{"date-parts":[[2019,5]]}},"alternative-id":["10.1136\/bcr-2018-229034"],"URL":"https:\/\/doi.org\/10.1136\/bcr-2018-229034","relation":{},"ISSN":["1757-790X"],"issn-type":[{"value":"1757-790X","type":"electronic"}],"subject":[],"published":{"date-parts":[[2019,5]]}}}