Historial de revisiones de «Gitelman syndrome»

19 mar 2026

• actant 11:3111:31 19 mar 2026‎ Danbot discusión contribs.‎ 7205 bytes +127‎ Added DDX template transclusions: Hypokalemia, Hypomagnesemia, Metabolic alkalosis, Renal tubular disorders, Prolonged QT
• actant 11:1411:14 19 mar 2026‎ Danbot discusión contribs.‎ 7078 bytes −385‎ Moved intro paragraph into Background section as bullets; removed excessive bold formatting from bullet lead-in text throughout

18 mar 2026

• actant 02:4002:40 18 mar 2026‎ Ostermayer discusión contribs.‎ 7463 bytes +7463‎ 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 '..."