Reactions Weekly

, Volume 1696, Issue 1, pp 362–362 | Cite as

Vitamin D

Idiopathic infantile hypercalcaemia and medullary nephrocalcinosis: case report
Case report


  1. Madsen JOB, et al. CYP24A1 mutation in a girl infant with idiopathic infantile hypercalcemia. JCRPE Journal of Clinical Research in Pediatric Endocrinology 10: 83-86, No. 1, Mar 2018. Available from: URL: -DenmarkCrossRefPubMedGoogle Scholar

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© Springer International Publishing AG, part of Springer Nature 2018

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