APRT DEFICIENCY
Clinical trials for APRT DEFICIENCY explained in plain language.
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Could a biobank unlock secrets of rare kidney stone diseases?
Knowledge-focused Recruiting nowThis study creates a biobank of blood, urine, and tissue samples from people with rare kidney stone diseases—primary hyperoxaluria, cystinuria, APRT deficiency, and Dent disease—and their family members. By storing these samples, researchers hope to enable future studies that cou…
Matched conditions: APRT DEFICIENCY
Sponsor: Mayo Clinic • Aim: Knowledge-focused
Last updated Jul 24, 2026 00:00 UTC
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Global registry aims to crack the code of rare kidney stone diseases
Knowledge-focused Recruiting nowThis study collects medical information from people around the world who have one of four rare hereditary kidney stone diseases: primary hyperoxaluria, Dent disease, cystinuria, or APRT deficiency. By gathering data from many patients, researchers hope to better understand how th…
Matched conditions: APRT DEFICIENCY
Sponsor: Mayo Clinic • Aim: Knowledge-focused
Last updated Jul 12, 2026 00:00 UTC