{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,2,21]],"date-time":"2026-02-21T05:32:12Z","timestamp":1771651932104,"version":"3.50.1"},"reference-count":12,"publisher":"Wiley","issue":"9","license":[{"start":{"date-parts":[[2016,9,29]],"date-time":"2016-09-29T00:00:00Z","timestamp":1475107200000},"content-version":"vor","delay-in-days":28,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Pediatrics International"],"published-print":{"date-parts":[[2016,9]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Neonatal Bartter syndrome (NBS) is a rare autosomal recessive renal tubular disorder. This disease is characterized by hypokalemia, hypochloremia, and metabolic alkalosis that is often associated with failure to thrive and recurrent episodes of dehydration. The combination of BS and cholelithiasis in an infant is very rare. Herein, we report a premature male infant with NBS who developed cholelithiasis and hydrocephalus on clinical follow up. We recommend that periodic routine hepatobiliary ultrasonograpic screening for cholelithiasis should be performed in patients with NBS.<\/jats:p>","DOI":"10.1111\/ped.12999","type":"journal-article","created":{"date-parts":[[2016,9,29]],"date-time":"2016-09-29T13:12:21Z","timestamp":1475154741000},"page":"912-915","source":"Crossref","is-referenced-by-count":6,"title":["Neonatal Bartter syndrome with cholelithiasis and hydrocephalus: Rare association"],"prefix":"10.1111","volume":"58","author":[{"given":"\u00d6zmert MA","family":"\u00d6zdemir","sequence":"first","affiliation":[{"name":"Department of Pediatrics Division of Neonatology Pamukkale University Faculty of Medicine  Denizli Turkey"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ceren","family":"\u00c7\u0131ral\u0131","sequence":"additional","affiliation":[{"name":"Department of Pediatrics Division of Neonatology Pamukkale University Faculty of Medicine  Denizli Turkey"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sebahat","family":"Y\u0131lmaz A\u011flad\u0131o\u011flu","sequence":"additional","affiliation":[{"name":"Department of Pediatric Endocrinology Division of Neonatology Pamukkale University Faculty of Medicine  Denizli Turkey"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Havva","family":"Evreng\u00fcl","sequence":"additional","affiliation":[{"name":"Department of Pediatric Nephrology Division of Neonatology Pamukkale University Faculty of Medicine  Denizli Turkey"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Emre","family":"Tepeli","sequence":"additional","affiliation":[{"name":"Department of Genetics Division of Neonatology Pamukkale University Faculty of Medicine  Denizli Turkey"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hacer","family":"Ergin","sequence":"additional","affiliation":[{"name":"Department of Pediatrics Division of Neonatology Pamukkale University Faculty of Medicine  Denizli Turkey"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2016,9,29]]},"reference":[{"key":"e_1_2_6_2_1","doi-asserted-by":"publisher","DOI":"10.1155\/2012\/857136"},{"key":"e_1_2_6_3_1","first-page":"229","article-title":"Neonatal Bartter syndrome","volume":"69","author":"Wong AC","year":"2014","journal-title":"Med. 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