Agrawal, S, Subedi, K, Ray, P and Rayamajhi, A
(2016)
Unusual case of failure to thrive: Type III Bartter syndrome.
Journal of Nepal Health Research Council, 14 (34).
pp. 210-213.
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Abstract
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.
Item Type: | Article |
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Uncontrolled Keywords: | Humans, Bartter Syndrome, Hypokalemia, Magnesium Deficiency, Failure to Thrive, Infant, Nepal, Female, Hypercalciuria |
Depositing User: | Symplectic Admin |
Date Deposited: | 01 Jul 2020 10:53 |
Last Modified: | 18 Jan 2023 23:48 |
Related URLs: | |
URI: | https://livrepository.liverpool.ac.uk/id/eprint/3091927 |