How to Cite
Abstract
Bartter Syndrome is an autosomal recessive hereditary renal tubular disorder, uncommon, affecting approximately 1 in 1,000,000 of the population. This syndrome is caused by homozygous or heterozygous mutations composed of four genes that encode proteins that participate in the tubular reabsorption of fluid in the thick ascending segment of the loop of Henle, causing an alteration in the reabsorption of sodium, potassium and chlorine, resulting in clinical manifestations of importance.
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References
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