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. 2019 Apr 29;4(6):893–897. doi: 10.1016/j.ekir.2019.04.016

Table 2.

Key teaching points

1. Timely diagnosis of the underlying etiology of nephrocalcinosis is important to halt progression of renal injury.
2. Genetic etiologies of nephrocalcinosis are particularly common in the pediatric setting.
3. CYP24A1 mutations are an autosomal recessive etiology of idiopathic infantile hypercalcemia and nephrocalcinosis.