{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,27]],"date-time":"2026-08-27T19:12:16Z","timestamp":1787857936263,"version":"build-2784847793"},"reference-count":14,"publisher":"Wiley","issue":"11","license":[{"start":{"date-parts":[[2011,4,25]],"date-time":"2011-04-25T00:00:00Z","timestamp":1303689600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Acta Paediatrica"],"published-print":{"date-parts":[[2011,11]]},"abstract":"Abstract<\/jats:title>Pseudo\u2010Bartter\u2019s (PB) syndrome characterized by hypokalemic metabolic alkalosis and persistent failure to thrive constitutes a rare typical presentation of cystic fibrosis (CF) with prevalence of 16.8%. We present a case of CF presenting with failure to thrive, dehydration, PB syndrome associated with chest infection and primo\u2010colonization with Pseudomonas aeruginosa.<\/jats:italic> Sweat chloride test was 102\u2003mmol\/L. DNA analysis identified 2 mutations 3849\u2003+\u20031G>A (intron 19) and 4382delA (exon 24) present in heterozygous status. To the best of our knowledge, our case is the first reported case in the literature of CF manifested by PB syndrome associated with chest infection and primo\u2010colonization with Pseudomonas aeruginosa.<\/jats:italic><\/jats:p>Conclusion:\u2002<\/jats:bold> The genotype 3849\u2003+\u20031G>A\/4382delA found in our patient is described for the first time in the literature. It explains the lung involvement with the dehydration and electrolyte disturbances. The role of the mutation in exon 24 in cases of CF with PB syndrome remains to be determined.<\/jats:p>","DOI":"10.1111\/j.1651-2227.2011.02294.x","type":"journal-article","created":{"date-parts":[[2011,3,30]],"date-time":"2011-03-30T13:19:22Z","timestamp":1301491162000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":9,"title":["Pseudo\u2010Bartter\u2019s syndrome revealing cystic fibrosis in an infant caused by 3849\u2003+\u20031G>A and 4382delA compound heterozygosity"],"prefix":"10.1111","volume":"100","author":[{"given":"El\u2010Rifai","family":"Nahida","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Hourani","family":"Mohammed","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lalau","family":"Guy","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2011,4,25]]},"reference":[{"key":"e_1_2_5_2_2","first-page":"33","article-title":"The case of pseudo\u2010Bartter\u2019s syndrome: an atypical presentation of cystic fibrosis","volume":"15","author":"\u017dianovi\u0107 S","year":"2008","journal-title":"Med Biol"},{"key":"e_1_2_5_3_2","volume-title":"Nelson textbook of pediatrics","author":"Kliegman RM","year":"2003"},{"key":"e_1_2_5_4_2","first-page":"38","article-title":"Elevated sweat potassium, hyeraldosteronism and pseudo Bartter\u2019s syndrome: a spectrum of disorders associated with cystic fibrosis","volume":"82","author":"Devlin J","year":"1989","journal-title":"J R Soc Med"},{"key":"e_1_2_5_5_2","first-page":"694","article-title":"Rare F311L CFTR gene mutation in a child presented with recurrent electrolyte abnormalities and metabolic alkalosis: case report","volume":"92","author":"Lumpaopong A","year":"2009","journal-title":"J Med Assoc Thai"},{"key":"e_1_2_5_6_2","doi-asserted-by":"publisher","DOI":"10.1097\/01.pec.0000245170.31343.bb"},{"key":"e_1_2_5_7_2","doi-asserted-by":"publisher","DOI":"10.1046\/j.1442-200X.2002.01563.x"},{"key":"e_1_2_5_8_2","doi-asserted-by":"publisher","DOI":"10.1002\/(SICI)1098-1004(200005)15:5<485::AID-HUMU22>3.0.CO;2-3"},{"key":"e_1_2_5_9_2","doi-asserted-by":"publisher","DOI":"10.1055\/s-2000-9650"},{"key":"e_1_2_5_10_2","doi-asserted-by":"publisher","DOI":"10.1016\/S0022-3476(95)70310-1"},{"key":"e_1_2_5_11_2","doi-asserted-by":"crossref","first-page":"242","DOI":"10.1093\/tropej\/50.4.242","article-title":"Pseudo\u2010Bartter\u2019s syndrome in an Egyptian infant with cystic fibrosis mutation N1303K","volume":"50","author":"Wahab AA","year":"2004","journal-title":"J Trop Pediatr"},{"key":"e_1_2_5_12_2","doi-asserted-by":"publisher","DOI":"10.1556\/OH.2008.28239"},{"key":"e_1_2_5_13_2","doi-asserted-by":"publisher","DOI":"10.1179\/146532805X45719"},{"key":"e_1_2_5_14_2","doi-asserted-by":"publisher","DOI":"10.1002\/humu.1998.11.4.337"},{"key":"e_1_2_5_15_2","doi-asserted-by":"publisher","DOI":"10.1034\/j.1399-0004.2003.00140.x"}],"container-title":["Acta Paediatrica"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1111%2Fj.1651-2227.2011.02294.x","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1111\/j.1651-2227.2011.02294.x","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,10,15]],"date-time":"2023-10-15T17:39:02Z","timestamp":1697391542000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1111\/j.1651-2227.2011.02294.x"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2011,4,25]]},"references-count":14,"journal-issue":{"issue":"11","published-print":{"date-parts":[[2011,11]]}},"alternative-id":["10.1111\/j.1651-2227.2011.02294.x"],"URL":"https:\/\/doi.org\/10.1111\/j.1651-2227.2011.02294.x","archive":["Portico"],"relation":{},"ISSN":["0803-5253","1651-2227"],"issn-type":[{"value":"0803-5253","type":"print"},{"value":"1651-2227","type":"electronic"}],"subject":[],"published":{"date-parts":[[2011,4,25]]},"assertion":[{"value":"2011-04-25","order":2,"name":"published","label":"Published","group":{"name":"publication_history","label":"Publication History"}}]}}