Idiopathic infantile hypercalcemia with severe nephrocalcinosis, associated with mutations: a case report
Nephrocalcinosis often occurs in infants and is caused by excessive calcium or vitamin D supplementation, neonatal primary hyperparathyroidism, and genetic disorders. Idiopathic infantile hypercalcemia (IIH), a rare cause of nephrocalcinosis, results from genetic defects in CYP24A1 or SLC34A1. Mutat...
| Published in: | Childhood Kidney Diseases |
|---|---|
| Main Authors: | , , |
| Format: | Article |
| Language: | English |
| Published: |
Korean Society of Pediatric Nephrology
2022-06-01
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| Subjects: | |
| Online Access: | http://www.chikd.org/upload/ckd-22-027.pdf |
