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...
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| Main Authors: | , , |
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| Format: | Book |
| Published: |
Korean Society of Pediatric Nephrology,
2022-06-01T00:00:00Z.
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| Call Number: |
A1234.567 |
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