Observational study reveals persistent nephrocalcinosis in children driven primarily by genetic disorders, highlighting the need for early diagnostic testing.
Congenital or genetic disorders are the primary causes of NC in children. Most cases persist overtime, underscoring the need for early identification of underlying causes through genetic testing and the development of more effective treatments for NC. While most children maintained normal renal function, the relationship between NC and renal functional decline warrants further investigation.
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Zheng et al. (2025) studied this question.
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