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Successful treatment of hypercalcaemia associated with a CYP24A1 mutation with fluconazole
Mutations in CYP24A1, encoding the vitamin D 24-hydroxlase enzyme, are known to cause a range of clinical phenotypes and presentations including idiopathic infantile hypercalcaemia and adult-onset nephrocalcinosis and nephrolithiasis. In the context of raised or borderline high serum calcium levels,...
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| Veröffentlicht in: | Clin Kidney J |
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| Hauptverfasser: | , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Oxford University Press
2015
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4515887/ https://ncbi.nlm.nih.gov/pubmed/26251716 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/ckj/sfv028 |
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