Abstract
Cystic fibrosis (CF) is an autosomal recessive genetic disorder. We report a case of a boy aged 4.5 years with cystic fibrosis, presenting under-weightness, hypocalcemia, metabolic alkalosis, hypokalemia, and hyponatremia. Sweat analysis of the patients concluded pseudo-Bartter syndrome, which was successfully treated using antibiotics, physiotherapy, fluids, vitamin supplements, and pancreatic enzyme therapy.
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APA
Faraji-Goodarzi, M. (2019). Pseudo-Bartter syndrome in children with cystic fibrosis. Clinical Case Reports, 7(6), 1123–1126. https://doi.org/10.1002/ccr3.2180
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