{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,13]],"date-time":"2026-10-13T02:21:05Z","timestamp":1791858065279,"version":"4.3.4"},"reference-count":12,"publisher":"SAGE Publications","issue":"8","license":[{"start":{"date-parts":[[1985,8,1]],"date-time":"1985-08-01T00:00:00Z","timestamp":491702400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Clin Pediatr (Phila)"],"published-print":{"date-parts":[[1985,8]]},"abstract":"<jats:p>Features suggestive of Bartter syndrome (hypokalemia, hypochloremic metabolic alkalosis, and normal blood pressure despite hyperreninemia and hyperaldoster onism) were found in a 5-year-old black child with cystinosis and Fanconi syndrome. Review of his medical records revealed that these abnormalities had probably been present when he first became clinically ill at 2 years of age. Sodium and potassium chloride supplementation lead to improved growth and strength, partial correction of his electrolyte abnormalities, and a decrease in markedly elevated plasma renin activity. Literature review disclosed a similar presentation in four Caucasian children with cystinosis.<\/jats:p>\n                  <jats:p>Biochemical findings compatible with Bartter syndrome can occur together with evidence of generalized proximal renal tubular dysfunction (Fanconi syn drome) in nephropathic cystinosis.<\/jats:p>","DOI":"10.1177\/000992288502400806","type":"journal-article","created":{"date-parts":[[2007,11,26]],"date-time":"2007-11-26T17:50:16Z","timestamp":1196099416000},"page":"447-451","source":"Crossref","is-referenced-by-count":19,"title":["Cystinosis Presenting with Features Suggesting Bartter Syndrome"],"prefix":"10.1177","volume":"24","author":[{"given":"Michael P.","family":"Whyte","sequence":"first","affiliation":[{"name":"Metabolic Research Unit, Shriners Hospital for Crippled Children, 2001 South Lindbergh Blvd., St. Louis, MO 63131"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sudah","family":"Shaheb","sequence":"additional","affiliation":[{"name":"From the Metabolic Research Unit, Shriners Hospitals for Crippled Children; the Division of Bone and Mineral Metabolism, Department of Medicine, The Jewish Hospital of St. Louis; Washington University School of Medicine; and Edward Mauinckrodt Department of Pediatrics, St. Louis ChHdren's Hospital, St. Louis, Missouri."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"H. William","family":"Schnaper","sequence":"additional","affiliation":[{"name":"From the Metabolic Research Unit, Shriners Hospitals for Crippled Children; the Division of Bone and Mineral Metabolism, Department of Medicine, The Jewish Hospital of St. Louis; Washington University School of Medicine; and Edward Mauinckrodt Department of Pediatrics, St. Louis ChHdren's Hospital, St. Louis, Missouri."}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"179","published-online":{"date-parts":[[1985,8,1]]},"reference":[{"key":"atypb1","unstructured":"Schneider JA, Schulman JD Cystinosis. In: Stanbury JB, Wyngaarden JB, Fredrickson DS, eds. Metabolic basis of inherited disease. 5th ed. New York: McGraw-Hill Book Company, Inc. 1983:1844-66."},{"key":"atypb2","first-page":"00","volume":"1","author":"Schneider JA","year":"1982","journal-title":"J Pediatr"},{"key":"atypb3","first-page":"117","volume":"151","author":"Jonas AJ","year":"1982","journal-title":"Johns Hopkins Med J"},{"key":"atypb4","doi-asserted-by":"publisher","DOI":"10.1038\/ki.1981.200"},{"key":"atypb5","doi-asserted-by":"publisher","DOI":"10.1159\/000181973"},{"key":"atypb6","doi-asserted-by":"publisher","DOI":"10.1016\/0002-9343(78)90794-5"},{"key":"atypb7","doi-asserted-by":"publisher","DOI":"10.1038\/ki.1981.12"},{"key":"atypb8","volume-title":"Syndrome de Bartter Associe a une cystinose (abstract)","author":"Lebel M.","year":"1977"},{"key":"atypb9","first-page":"1825","volume":"30","author":"Berio A.","year":"1978","journal-title":"Pediatr"},{"key":"atypb10","doi-asserted-by":"publisher","DOI":"10.1203\/00006450-197804001-01090"},{"key":"atypb11","first-page":"51","volume":"33","author":"O'Regan S.","year":"1980","journal-title":"Acta Pediatr Belg"},{"key":"atypb12","doi-asserted-by":"publisher","DOI":"10.1016\/0002-9343(68)90066-1"}],"container-title":["Clinical Pediatrics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/journals.sagepub.com\/doi\/pdf\/10.1177\/000992288502400806","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/journals.sagepub.com\/doi\/pdf\/10.1177\/000992288502400806","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,4,28]],"date-time":"2026-04-28T16:26:28Z","timestamp":1777393588000},"score":1,"resource":{"primary":{"URL":"https:\/\/journals.sagepub.com\/doi\/10.1177\/000992288502400806"}},"subtitle":["Case Report and Literature Review"],"short-title":[],"issued":{"date-parts":[[1985,8]]},"references-count":12,"journal-issue":{"issue":"8","published-print":{"date-parts":[[1985,8]]}},"alternative-id":["10.1177\/000992288502400806"],"URL":"https:\/\/doi.org\/10.1177\/000992288502400806","relation":{},"ISSN":["0009-9228","1938-2707"],"issn-type":[{"value":"0009-9228","type":"print"},{"value":"1938-2707","type":"electronic"}],"subject":[],"published":{"date-parts":[[1985,8]]}}}