Registry for inherited rare kidney stone disorders
Part of Genetic & congenital, Hormones & metabolism, Kidney & urinary, Women’s health & pregnancy clinical trials.
This registry collects information from people with certain inherited rare kidney stone conditions. It helps researchers learn about the conditions and supports future studies that may improve care.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You must have a confirmed diagnosis of one of these: Primary Hyperoxaluria, Dent Disease, Cystinuria, or APRT Deficiency
- You must have a family history of a sibling with one of these same conditions
- If you do not have one of these specific diagnoses, you likely cannot join
Quick eligibility check
Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.
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