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Published in 2017 at "Kidney international"
DOI: 10.1016/j.kint.2016.09.046
Abstract: Gitelman syndrome (GS) is a rare, salt-losing tubulopathy characterized by hypokalemic metabolic alkalosis with hypomagnesemia and hypocalciuria. The disease is recessively inherited, caused by inactivating mutations in the SLC12A3 gene that encodes the thiazide-sensitive sodium-chloride…
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Keywords:
syndrome consensus;
gitelman syndrome;
disease;
consensus guidance ... See more keywords