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SAT-368 CYP24A1 Mutation Masking Malignancy Mediated Hypercalcemia
Background: Mutations in CYP24A1, resulting in reduced conversion of 1,25(OH)(2)D to its inactive metabolite 24,25-(OH)(2)D(3),are rare causes of parathyroid hormone (PTH)-independent hypercalcemia. While manifestations may range from the severe idiopathic infantile hypercalcemia due to biallelic mu...
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| Publicado en: | J Endocr Soc |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Oxford University Press
2020
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7208999/ https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jendso/bvaa046.353 |
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