Gitelman syndrome: Revision history

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19 March 2026

18 March 2026

  • curprev 02:4002:40, 18 March 2026‎ Ostermayer talk contribs‎ 7,463 bytes +7,463‎ Created page with "Gitelman syndrome is an autosomal recessive salt-losing tubulopathy caused by loss-of-function mutations in the '''thiazide-sensitive sodium-chloride cotransporter (NCC)''' in the distal convoluted tubule.<ref name="StatPearls">Gitelman Syndrome. ''StatPearls''. NCBI. 2024.</ref> It is the '''most common inherited renal tubulopathy''' (~1 in 40,000) and presents with '''hypokalemic metabolic alkalosis, hypomagnesemia, and hypocalciuria''' — biochemically identical to '..."
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