Familial juvenile hyperuricemic nephropathy type 1
MONDO:0008073A rare kidney disorder characterized by hyperuricemia, progressive nephropathy, and gout occurring at an early age.
Also known as: familial juvenile gouty nephropathy, familial nephropathy with gout, gouty nephropathy, familial juvenile, hyperuricemic nephropathy, familial juvenile, nephropathy, familial, with gout, ADTKD-UMOD, Autosomal Dominant Tubulo-Interstitial Kidney Disease, FJHN type 1
2 clinical trials for this condition and its sub-types, 0 tagged with Familial juvenile hyperuricemic nephropathy type 1 itself.
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Could a diabetes drug protect kidneys in children with genetic disease?
Disease control Recruiting nowThis 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
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Scientists launch major study to unravel mysterious metabolism disorders
Knowledge-focused Recruiting nowThis study aims to learn more about rare disorders that affect how the body processes chemicals called pyrimidines and purines. These disorders can cause problems in the brain, blood, kidneys, and immune system, ranging from mild to life-threatening. Researchers will compare test…
Sponsor: National Human Genome Research Institute (NHGRI) • Aim: Knowledge-focused
Last updated Aug 21, 2026 00:00 UTC