{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,27]],"date-time":"2026-08-27T19:12:13Z","timestamp":1787857933461,"version":"build-2784847793"},"reference-count":25,"publisher":"Japanese Society for Pediatric Endocrinology","issue":"3","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Clin Pediatr Endocrinol"],"published-print":{"date-parts":[[2023]]},"DOI":"10.1297\/cpe.2022-0069","type":"journal-article","created":{"date-parts":[[2023,3,18]],"date-time":"2023-03-18T18:10:29Z","timestamp":1679163029000},"page":"155-160","source":"Crossref","is-referenced-by-count":2,"title":["Pseudo-Bartter syndrome in an infant without obvious underlying conditions: A          case report"],"prefix":"10.1297","volume":"32","author":[{"given":"Junya","family":"Toyoda","sequence":"first","affiliation":[{"name":"Department of Pediatrics, Showa University School of              Medicine, Tokyo, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Masanori","family":"Adachi","sequence":"additional","affiliation":[{"name":"Department of Pediatrics, Showa University School of              Medicine, Tokyo, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ayako","family":"Ochi","sequence":"additional","affiliation":[{"name":"Department of Pediatrics, Showa University School of              Medicine, Tokyo, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yuki","family":"Okada","sequence":"additional","affiliation":[{"name":"Department of Pediatrics, Showa University School of              Medicine, Tokyo, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Aiko","family":"Honda","sequence":"additional","affiliation":[{"name":"Department of Pediatrics, Showa University School of              Medicine, Tokyo, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Katsumi","family":"Mizuno","sequence":"additional","affiliation":[{"name":"Department of Pediatrics, Showa University School of              Medicine, Tokyo, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kandai","family":"Nozu","sequence":"additional","affiliation":[{"name":"Department of Pediatrics, Kobe University Graduate              School of Medicine, Kobe, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"125","reference":[{"key":"1","doi-asserted-by":"crossref","unstructured":"1. Matsunoshita,                N, Nozu,                K, Shono,                A, Nozu,                Y, Fu,                XJ,                Morisada,            N, et al.            Differential diagnosis of Bartter syndrome, Gitelman syndrome, and            pseudo-Bartter\/Gitelman syndrome based on clinical characteristics.            Genet Med          2016;18: 180\u20138.","DOI":"10.1038\/gim.2015.56"},{"key":"2","doi-asserted-by":"crossref","unstructured":"2. Mantoo,              MR, Kabra,                M, Kabra,                SK. Cystic            fibrosis presenting as pseudo-Bartter syndrome: An important diagnosis that is            missed!Indian J Pediatr          2020;87: 726\u201332.","DOI":"10.1007\/s12098-020-03342-8"},{"key":"3","doi-asserted-by":"crossref","unstructured":"3. Konrad,              M, Nijenhuis,                T, Ariceta,                G,                Bertholet-Thomas,              A, Calo,                LA,              Capasso, G,              et al. Diagnosis and management of Bartter            syndrome: executive summary of the consensus and recommendations from the European Rare            Kidney Disease Reference Network Working Group for Tubular Disorders.            Kidney Int          2021;99: 324\u201335.","DOI":"10.1016\/j.kint.2020.10.035"},{"key":"4","doi-asserted-by":"crossref","unstructured":"4. Nozu,              K, Yamamura,                T,                Horinouchi,              T, Nagano,                C,                Sakakibara,              N, Ishikura,                K, et al.            Inherited salt-losing tubulopathy: An old condition but a new category of            tubulopathy. Pediatr Int          2020;62: 428\u201337.","DOI":"10.1111\/ped.14089"},{"key":"5","doi-asserted-by":"crossref","unstructured":"5. Jdiaa,              SS, Walsh,                SB,                Bockenhauer,              D,              Fakhredine,              SW, Koubar,                SH. The            hypokalemia mystery: distinguishing Gitelman and Bartter syndromes from \u2018pseudo-Bartter            syndrome\u2019. Nephrol Dial Transplant          2021;37: 29\u201330.","DOI":"10.1093\/ndt\/gfaa100"},{"key":"6","doi-asserted-by":"crossref","unstructured":"6. Schimert,                P,                Bernet-Buettiker,              V,                Rutishauser,              C, Schams,                M, Frey,                B.            Transplacental metabolic alkalosis. J Paediatr            Child Health          2007;43: 851\u20133.","DOI":"10.1111\/j.1440-1754.2007.01239.x"},{"key":"7","doi-asserted-by":"crossref","unstructured":"7. Babatseva,                E,                Chatziioannidis,              I, Tagaraki,                AA, Tramma,                D, Dampala,                K,                Chatzitoliou,              E, et al.            A neonate with intrauterine growth restriction and pseudo-Bartter            syndrome due to severe maternal eating disorder: A case report.            Clin Case Rep          2020;8: 2541\u20134.","DOI":"10.1002\/ccr3.3223"},{"key":"8","doi-asserted-by":"crossref","unstructured":"8. Najafi,              M,                Kordi-Tamandani,              DM, Behjati,                F,                Sadeghi-Bojd,              S, Bakey,                Z,                Karimiani,              EG, et al.            Mimicry and well known genetic friends: molecular diagnosis in an Iranian            cohort of suspected Bartter syndrome and proposition of an algorithm for clinical            differential diagnosis. Orphanet J Rare Dis          2019;14: 41.","DOI":"10.1186\/s13023-018-0981-5"},{"key":"9","doi-asserted-by":"crossref","unstructured":"9. Matsunoshita,                N, Nozu,                K,                Yoshikane,              M, Kawaguchi,                A, Fujita,                N,              Morisada, N,              et al. Congenital chloride diarrhea needs            to be distinguished from Bartter and Gitelman syndrome. J Hum            Genet          2018;63: 887\u201392.","DOI":"10.1038\/s10038-018-0470-7"},{"key":"10","doi-asserted-by":"crossref","unstructured":"10. Vilotijevi\u0107-Dautovi\u0107,                G,                Stojanovi\u0107,              V.            Pseudo-Bartter\u2019s syndrome in patients with cystic fibrosis: A case series            and review of the literature. Srp Arh Celok Lek          2015;143: 748\u201351.","DOI":"10.2298\/SARH1512748V"},{"key":"11","doi-asserted-by":"crossref","unstructured":"11. Shetty,              AK, Rogers,                NL,              Mannick, EE,                Aviles,            DH. Syndrome of            hypokalemic metabolic alkalosis and hypomagnesemia associated with gentamicin therapy:            case reports. Clin Pediatr (Phila)          2000;39: 529\u201333.","DOI":"10.1177\/000992280003900904"},{"key":"12","doi-asserted-by":"crossref","unstructured":"12. Chen,              Q, Cao,                Y, Xu,                L, Liu,                J, Wu,                X.            Bartter-like syndrome as the initial presentation of Dent disease 1: A            case report. Front Pediatr          2021;9: 725251.","DOI":"10.3389\/fped.2021.725251"},{"key":"13","unstructured":"13. Yu,                HR, Huang,                SC, Hsieh,                CS. Infantile            hypertrophic pyloric stenosis presenting as pseudo-Bartter\u2019s syndrome and seizures:            report of one case. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za            Zhi          1998;39: 195\u20137."},{"key":"14","doi-asserted-by":"crossref","unstructured":"14. Signorelli,                GC,                Bianchetti,              MG, Jermini,                LMM,                Agostoni,            C, Milani,                GP,                Simonetti,              GD, et al.            Dietary chloride deficiency syndrome: Pathophysiology, history, and            systematic literature review. Nutrients          2020;12: 3436.","DOI":"10.3390\/nu12113436"},{"key":"15","doi-asserted-by":"crossref","unstructured":"15. Kato,              N, Takimoto,                H, Sudo,                N. The cubic            functions for spline smoothed L, S and M values for BMI reference data of Japanese            children. Clin Pediatr Endocrinol          2011;20: 47\u20139.","DOI":"10.1297\/cpe.20.47"},{"key":"16","doi-asserted-by":"publisher","unstructured":"16. Task Force on Blood Pressure Control            in Children. Report of the second task force on blood            pressure control in children\u20131987. National Heart, Lung,            and Blood Institute, Bethesda, Marylan. Pediatrics          1987;79: 1\u201325.","DOI":"10.1542\/peds.79.1.1"},{"key":"17","doi-asserted-by":"crossref","unstructured":"17. Enver,              EO,                Vatansever,              P, Guran,                O, Bilgin,                L, Boran,                P, Turan,                S, et al.            Adrenal steroids reference ranges in infancy determined by            LC-MS\/MS. Pediatr Res          2022;92: 265\u201374.","DOI":"10.1038\/s41390-021-01739-5"},{"key":"18","doi-asserted-by":"crossref","unstructured":"18. Mersin,              SS, Ramelli,                GP,                Laux-End,            R, Bianchetti,                MG. Urinary            chloride excretion distinguishes between renal and extrarenal metabolic            alkalosis. Eur J Pediatr          1995;154: 979\u201382.","DOI":"10.1007\/BF01958641"},{"key":"19","doi-asserted-by":"crossref","unstructured":"19. Bettinelli,                A, Borsa,                N,                Bellantuono,              R, Syr\u00e8n,                ML,                Calabrese,              R, Edefonti,                A, et al.            Patients with biallelic mutations in the chloride channel gene CLCNKB:            long-term management and outcome. Am J Kidney Dis          2007;49: 91\u20138.","DOI":"10.1053\/j.ajkd.2006.10.001"},{"key":"20","doi-asserted-by":"crossref","unstructured":"20. Muhammad,                E,                Leventhal,              N, Parvari,                G,                Hanukoglu,              A, Hanukoglu,                I,                Chalifa-Caspi,              V, et al.            Autosomal recessive hyponatremia due to isolated salt wasting in sweat            associated with a mutation in the active site of Carbonic Anhydrase 12.            Hum Genet          2011;129: 397\u2013405.","DOI":"10.1007\/s00439-010-0930-4"},{"key":"21","doi-asserted-by":"crossref","unstructured":"21. Miyahara,                J, Aramaki,                S, Yokochi,                K. Dietary            chloride deficiency due to new liquid nutritional products.            Pediatr Int          2009;51: 197\u2013200.","DOI":"10.1111\/j.1442-200X.2008.02670.x"},{"key":"22","doi-asserted-by":"crossref","unstructured":"22. EFSA Panel on Dietetic Products,            Nutrition and Allergies (NDA), European Food Safety Authority (EFSA).            Scientific Opinion on nutrient requirements and dietary intakes of            infants and young children in the European Union. EFSA            J          2013;11: 3408.","DOI":"10.2903\/j.efsa.2013.3408"},{"key":"23","unstructured":"23. Institute of Medicine          2005. Dietary reference intakes for water, potassium, sodium, chloride, and          sulfate. Washington, DC: The National Academies Press.            https:\/\/doi.org\/."},{"key":"24","unstructured":"24. Dietary Reference Intakes for            Japanese ( 2020 Edition) Review Committee Report (In          Japanese). https:\/\/www.mhlw.go.jp\/content\/10904750\/000586577.pdf (accessed on 14 Feb.          2023)."},{"key":"25","doi-asserted-by":"crossref","unstructured":"25. Maalouf,              J, Cogswell,                ME, Yuan,                K, Martin,                C, Gunn,                JP,                Pehrsson,            P, et al.            Top sources of dietary sodium from birth to age 24 mo, United States,            2003-2010. Am J Clin Nutr          2015;101: 1021\u20138.","DOI":"10.3945\/ajcn.114.099770"}],"container-title":["Clinical Pediatric Endocrinology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.jstage.jst.go.jp\/article\/cpe\/32\/3\/32_2022-0069\/_pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,6,24]],"date-time":"2023-06-24T00:14:52Z","timestamp":1687565692000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.jstage.jst.go.jp\/article\/cpe\/32\/3\/32_2022-0069\/_article"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2023]]},"references-count":25,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2023]]}},"URL":"https:\/\/doi.org\/10.1297\/cpe.2022-0069","relation":{},"ISSN":["0918-5739","1347-7358"],"issn-type":[{"value":"0918-5739","type":"print"},{"value":"1347-7358","type":"electronic"}],"subject":[],"published":{"date-parts":[[2023]]},"article-number":"2022-0069"}}