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dc.contributor.authorAgrawal, Sumit-
dc.contributor.authorSubedi, Krishnahari-
dc.contributor.authorRay, Pankaj-
dc.contributor.authorRayamajhi, Ajit-
dc.identifier.citationAgrawalS., SubediK., RayP., & RayamajhiA. (2017). Unusual case of failure to thrive: Type III Bartter syndrome. Journal of Nepal Health Research Council, 14(3).
dc.identifier.issnPrint ISSN: 1727-5482; Online ISSN: 1999-6217-
dc.descriptionCase Reporten_US
dc.description.abstractAbstract Bartter syndrome Type III is a rare autosomal recessive disorder resulting from an inherited defect in the thick ascending limb of the loop of henle of the nephrons in kidney. The typical clinical manifestations in childhood are failure to thrive and recurrent episodes of vomiting. Typical laboratory findings which help in the diagnosis are hypokalemic metabolic alkalosis, hypomagnesemia and hypercalciuria. We report a case of Type III Bartter syndrome not responding to repeated conventional treatment of failure to thrive. Keywords: Bartter syndrome; failure to thrive; hypercalciuria; hypomagnesemia; hypokalemiaen_US
dc.publisherNepal Health Research Councilen_US
dc.relation.ispartofseriesSep-Dec, 2016;880-
dc.subjectBartter syndromeen_US
dc.subjectFailure to thriveen_US
dc.titleUnusual case of failure to thrive: Type III Bartter syndromeen_US
dc.typeJournal Articleen_US
local.journal.categoryCase Report-
Appears in Collections:Vol. 14 No. 3 Issue 34 Sep-Dec 2016

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