NighatASairaWLNasrulHS. ShakilARAbdulGB. Failure to thrive, can this be Bartter’s syndrome?J Dow Univ Health Sci. 2011;5:37-40.
2.
ThabetMSharakiOAFathyHMAyoubAZZ. Clinical and laboratory study of infants and children with Bartter syndrome attending Alexandria University Children’s Hospital (10 years experience). Alex J Pediatr. 2017;30:1-10.
3.
KonradMVollmerMLemminkHH, et al. Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome. J Am Soc Nephrol. 2000;11:1449-1459.
Rodriguez-SorianoJ. Bartter and related syndromes: the puzzle is almost solved. Pediatr Neprol. 1998;12:315-327.
7.
Al ShibliANarchiH. Bartter and Gitelman syndromes: spectrum of clinical manifestations caused by different mutations. World J Methodol. 2015;5:55-61.
8.
ChengCJLoYFChenJCHuangCLLinSH. Functional severity if CLCNKB mutations correlates with phenotypes in patients with classic Bartter’s syndrome. J Physiol. 2017;595:5573-5586.
9.
BrochardKBoyerOBlanchardA, et al. Phenotype-genotype correlation in antenatal and neonatal variants of Bartter syndrome. Nephrol Dial Transplant. 2009;24:1455-1464.
10.
CastanoAGde NanclaresGPMadariagaL, et al. Genetics of type III Bartter syndrome in Spain, proposed diagnostic algorithm. PLoS One. 2013;8:e74673.
11.
VieiraHMendesLMendesPda SilvaJE. Classic Bartter syndrome: a rare cause of failure to thrive in a child. BMJ Case Rep. 2012;2012:bcr0220125888. doi:10.1136/bcr.02.2012.5888
12.
Rodriguez-SorianoJ. Bartter’s syndrome comes of age. Pediatrics. 1999;103:663-664.
13.
AlhammadiAHKhalifaMAlnaimiL. An infant with poor weight gain and hypochloremic metabolic alkalosis: a case report. Int J Gen Med. 2014;7:389-391.
14.
ZelikovicISzargelRHawashA, et al. A novel mutation in the chloride channel gene, CLCNKB, as a cause of Gitelman and Bartter syndromes. Kidney Int. 2003;63:24-32.
15.
GavhaneJMarkandaKDograSJafriN. Severe metabolic alkalosis in an infant: Bartter syndrome. MGM J Med Sci. 2017;4:43-45.
