Genetic testing enables a precision medicine approach for nephrolithiasis and nephrocalcinosis in pediatrics: a single-center cohort.

Mol Genet Genomics · 2022 · PMC9250473 · PMID 35612621

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Hypercalciuria is the most common metabolic abnormality detected in children with NL or NC, and is especially highly significant for recurrent NL or progressive NC (Gürgöze and Sarı 2011 ; Saitz et al. 2017 ; Spivacow et al. 2008 ).

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