Loss of function mutations of CYP24A1 gene, which is involved in vitamin D catabolism, cause vitamin D-mediated PTH-independent hypercalcemia. The phenotype varies from life-threatening forms in the infancy to milder forms in the adulthood.

Hereditary hypercalcemia caused by a homozygous pathogenic variant in the cyp24a1 gene: A case report and review of the literature / Cappellani, D.; Brancatella, A.; Kaufmann, M.; Minucci, A.; Vignali, E.; Canale, D.; De Paolis, E.; Capoluongo, Ettore Domenico; Cetani, F.; Jones, G.; Marcocci, C.. - In: CASE REPORTS IN ENDOCRINOLOGY. - ISSN 2090-6501. - 2019:(2019), pp. 4982621-4982627. [10.1155/2019/4982621]

Hereditary hypercalcemia caused by a homozygous pathogenic variant in the cyp24a1 gene: A case report and review of the literature

Capoluongo;
2019

Abstract

Loss of function mutations of CYP24A1 gene, which is involved in vitamin D catabolism, cause vitamin D-mediated PTH-independent hypercalcemia. The phenotype varies from life-threatening forms in the infancy to milder forms in the adulthood.
2019
Hereditary hypercalcemia caused by a homozygous pathogenic variant in the cyp24a1 gene: A case report and review of the literature / Cappellani, D.; Brancatella, A.; Kaufmann, M.; Minucci, A.; Vignali, E.; Canale, D.; De Paolis, E.; Capoluongo, Ettore Domenico; Cetani, F.; Jones, G.; Marcocci, C.. - In: CASE REPORTS IN ENDOCRINOLOGY. - ISSN 2090-6501. - 2019:(2019), pp. 4982621-4982627. [10.1155/2019/4982621]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/777995
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