Pseudo-Bartter syndrome in children with cystic fibrosis.
Mojgan Faraji-GoodarziPublished in: Clinical case reports (2019)
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.
Keyphrases
- cystic fibrosis
- end stage renal disease
- case report
- ejection fraction
- newly diagnosed
- pseudomonas aeruginosa
- chronic kidney disease
- prognostic factors
- young adults
- peritoneal dialysis
- genome wide
- gene expression
- lung function
- patient reported outcomes
- stem cells
- heart failure
- dna methylation
- chronic obstructive pulmonary disease
- bone marrow
- atrial fibrillation