{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,8,28]],"date-time":"2025-08-28T10:10:01Z","timestamp":1756375801647,"version":"3.44.0"},"reference-count":15,"publisher":"BMJ","content-domain":{"domain":["bmj.com"],"crossmark-restriction":true},"short-container-title":["BMJ Case Reports"],"accepted":{"date-parts":[[2017,11,3]]},"abstract":"<jats:p>Antenatal Bartter syndrome is a rare condition that can present with different clinical features. These features include early onset maternal polyhydramnios, failure to thrive, prematurity and nephrocalcinosis.<\/jats:p>\n               <jats:p>We are presenting this 20-day-old girl who had an antenatal history of polyhydramnios. She developed persistent non-bilious vomiting that was associated with constipation soon after birth. She presented with failure to thrive and features suggestive of intestinal obstruction. On the initial evaluation, she was noted to have hypokalaemic, hyponatraemic metabolic alkalosis. The initial work-up was done to exclude surgical and renal causes of her presentation, and the diagnosis was confirmed by gene analysis to be type III\u2014classic Bartter syndrome. She was closely monitored for her growth and development with the appropriate salt replacement therapy.<\/jats:p>","DOI":"10.1136\/bcr-2017-221062","type":"journal-article","created":{"date-parts":[[2017,11,15]],"date-time":"2017-11-15T00:45:26Z","timestamp":1510706726000},"page":"bcr-2017-221062","update-policy":"https:\/\/doi.org\/10.1136\/crossmarkpolicy","source":"Crossref","is-referenced-by-count":1,"title":["Antenatal Bartter syndrome presenting with vomiting and constipation mimicking subacute intestinal obstruction in a 20-day-old neonate"],"prefix":"10.1136","volume":"2017","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-8676-0953","authenticated-orcid":false,"given":"Ibtihal Siddiq","family":"Abdelgadir","sequence":"first","affiliation":[{"name":"Department of Paediatric Emergency, Sidra Medical and Research Center, Doha, Qatar"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Fawzia","family":"Elgharbawy","sequence":"additional","affiliation":[{"name":"Hamad Medical Corporation, Doha, Qatar"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Khalil Mohamad","family":"Salameh","sequence":"additional","affiliation":[{"name":"Department of Paediatrics, Hamad Medical Corporation, Doha, Qatar"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Baha Eldin","family":"Juma","sequence":"additional","affiliation":[{"name":"Hamad Medical Corporation, Doha, Qatar"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","published-online":{"date-parts":[[2017,11,14]]},"reference":[{"key":"2025082802363374000_2017.nov14_1.bcr-2017-221062.1","doi-asserted-by":"publisher","DOI":"10.1007\/s00467-011-1871-4"},{"key":"2025082802363374000_2017.nov14_1.bcr-2017-221062.2","doi-asserted-by":"publisher","DOI":"10.1093\/ndt\/gfn689"},{"key":"2025082802363374000_2017.nov14_1.bcr-2017-221062.3","doi-asserted-by":"publisher","DOI":"10.1053\/j.ajkd.2006.10.001"},{"key":"2025082802363374000_2017.nov14_1.bcr-2017-221062.4","doi-asserted-by":"publisher","DOI":"10.1038\/ng1096-152"},{"key":"2025082802363374000_2017.nov14_1.bcr-2017-221062.5","doi-asserted-by":"publisher","DOI":"10.1007\/s00467-006-0062-1"},{"key":"2025082802363374000_2017.nov14_1.bcr-2017-221062.6","doi-asserted-by":"crossref","first-page":"180","DOI":"10.1038\/gim.2015.56","article-title":"Differential diagnosis of Bartter syndrome, Gitelman syndrome, and pseudo-Bartter\/Gitelman syndrome based on clinical characteristics","volume":"18","author":"Matsunoshita","year":"2016","journal-title":"Genet Med"},{"key":"2025082802363374000_2017.nov14_1.bcr-2017-221062.7","doi-asserted-by":"publisher","DOI":"10.1155\/2012\/479242"},{"key":"2025082802363374000_2017.nov14_1.bcr-2017-221062.8","first-page":"735","article-title":"Neonatal Bartter Syndrome-Case Reports","volume":"43","author":"Kumar","year":"2006","journal-title":"Indian Ped"},{"key":"2025082802363374000_2017.nov14_1.bcr-2017-221062.9","doi-asserted-by":"publisher","DOI":"10.1007\/s004670050461"},{"key":"2025082802363374000_2017.nov14_1.bcr-2017-221062.10","first-page":"335","article-title":"[Blood and urinary aldosterone levels in normal neonates, infants and children]","volume":"36","author":"Loeuille","year":"1981","journal-title":"Pediatrie"},{"key":"2025082802363374000_2017.nov14_1.bcr-2017-221062.11","doi-asserted-by":"publisher","DOI":"10.1203\/PDR.0b013e3181b1bbec"},{"key":"2025082802363374000_2017.nov14_1.bcr-2017-221062.12","doi-asserted-by":"crossref","first-page":"943","DOI":"10.1515\/jpem-2014-0188","article-title":"Antenatal Bartter syndrome presenting as hyperparathyroidism with hypercalcemia and hypercalciuria: a case report and review","volume":"28","author":"Gross","year":"2015","journal-title":"J Pediatr Endocrinol Metab"},{"key":"2025082802363374000_2017.nov14_1.bcr-2017-221062.13","doi-asserted-by":"crossref","first-page":"299","DOI":"10.1046\/j.1442-200x.1999.01056.x","article-title":"Bartter\u2019s syndrome in Arabic children: review of 13 cases","volume":"41","author":"Abdel-al","year":"1999","journal-title":"Pediatr Int"},{"key":"2025082802363374000_2017.nov14_1.bcr-2017-221062.14","first-page":"2393","article-title":"Familial aggregation and heritability of pyloric stenosis","volume":"2010","author":"Krogh","year":"2013","journal-title":"JAMA"},{"key":"2025082802363374000_2017.nov14_1.bcr-2017-221062.15","unstructured":"Sreedharan R , Anver ED . et al Bartter- Gitelman syndrome and other inherited tubular transport abnormalities. In: Kleigman RM , Stanton BF , St Geme III JW , Schor NF , . eds. Nelson Textbook of Pediatrics. 20th\u00a0edition. Saunders, Philadelphia, Pa, USA, 2016:2533\u20133."}],"container-title":["BMJ Case Reports"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/syndication.highwire.org\/content\/doi\/10.1136\/bcr-2017-221062","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,8,28]],"date-time":"2025-08-28T09:36:43Z","timestamp":1756373803000},"score":1,"resource":{"primary":{"URL":"https:\/\/casereports.bmj.com\/lookup\/doi\/10.1136\/bcr-2017-221062"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2017,11,14]]},"references-count":15,"alternative-id":["10.1136\/bcr-2017-221062"],"URL":"https:\/\/doi.org\/10.1136\/bcr-2017-221062","relation":{},"ISSN":["1757-790X"],"issn-type":[{"type":"electronic","value":"1757-790X"}],"subject":[],"published":{"date-parts":[[2017,11,14]]}}}