Nephrolithiasis is a common disorder, with a rising prevalence in the general population. Its pathogenesis is still unclear, but a role for genetics has long been recognized, especially in cases of the more common calcium nephrolithiasis. Although relatively rare, monogenic causes of hypercalciuria and nephrolithiasis do exist and their timely recognition is important from a prognostic and therapeutic viewpoint. This article reviews the clinical and laboratory findings characterizing inherited causes of nephrolithiasis with a view to helping clinicians to recognize and manage these rare conditions. © 2012 The Author.
CITATION STYLE
Ferraro, P. M., D’Addessi, A., & Gambaro, G. (2013). When to suspect a genetic disorder in a patient with renal stones, and why. Nephrology Dialysis Transplantation, 28(4), 811–820. https://doi.org/10.1093/ndt/gfs545
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