Cure My Disease

Don't miss your cure!

Home News Browse Soon ready About
Log in / Sign up

Isolated autosomal dominant hypomagnesemia, Glaudemans type

MONDO:0016048

Isolated autosomal dominant hypomagnesemia, Glaudemans type (IADHG) is a form of familial primary hypomagnesemia (FPH), characterized by low serum magnesium (Mg) values but normal urinary Mg values. The typical clinical features are recurrent muscle cramps, episodes of tetany, tremor, and muscle weakness, especially in distal limbs. The disease is potentially fatal.

1 clinical trial for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Disease (680) Metabolic disease (233) Kidney disorder (214) Hereditary disease (176) Urinary system disorder (66) Inborn errors of metabolism (45) Human disease (14) Familial primary hypomagnesemia (4) Disease of genetic or genomic mechanism (2) Inborn metal metabolism disorder (1)
Trials to join now! 1
Sort by
  • 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: PHASE3 • Sponsor: Children's Hospital of Fudan University • Aim: Disease control

    Last updated Jul 08, 2026 00:00 UTC

Cure My Disease

Helping patients find clinical trials that match their disease.

Why was Cure my disease built?

Explore

Home News Browse About Terms of use Contact us

This is a site from Cyber and Space