Gitelman syndrome

MONDO:0009904

Gitelman syndrome (GS), also referred to as familial hypokalemia-hypomagnesemia, is characterized by hypokalemic metabolic alkalosis in combination with significant hypomagnesemia and low urinary calcium excretion.

Also known as: Gitelman syndrome, hypomagnesemia-hypokalemia, primary renotubular, with hypocalciuria, primary renal tubular hypokalemic hypomagnesemia with hypocalciuria, GTLMNS, Gitelman's syndrome, Potassium and magnesium depletion, familial hypokalemia-hypomagnesemia

1 clinical trial for this condition and its sub-types, 0 tagged with Gitelman syndrome itself.

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Where it sits in the disease tree

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Part of

↑ Syndromic disease (7133) ↑ Inherited renal tubular disease (40) ↑ Renal tubular transport disease (17)

Including sub-types (1) Tagged with Gitelman syndrome (0)

Trials to join now! 1

Could a diabetes drug protect kidneys in children with genetic disease?

Disease control Recruiting now

This study tests whether adding dapagliflozin (a diabetes drug) to standard care reduces protein leakage in the urine of children with hereditary kidney diseases. About 44 children will receive either dapagliflozin plus standard care or standard care alone for 12 weeks, then swit…

Phase 3 • Sponsor: Children's Hospital of Fudan University • Aim: Disease control

Last updated Jul 08, 2026 00:00 UTC

Gitelman syndrome

Where it sits in the disease tree

Could a diabetes drug protect kidneys in children with genetic disease?