Gitelman syndrome: an analysis of the underlying pathophysiologic mechanisms of acid–base and electrolyte abnormalities
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DOI: 10.1007/s11255-017-1653-4
Abstract: Gitelman syndrome is the most common inherited tubular disease resulting from mutations of the SLC12A3 gene that encodes the thiazide-sensitive sodium–chloride cotransporter in the early distal convoluted tubules. The review presents the underlying pathophysiologic mechanisms… read more here.
Keywords: base electrolyte; underlying pathophysiologic; mechanisms acid; acid base ... See more keywords