THU472 Novel And Multifactorial Case Of Severe Hypercalcemia Due To Primary Hyperparathyroidism And Heterozygous Mutation Of CYP24A1

Disclosure: J. Liu: None. P. Angelos: None. M. Barhoum: None. R. Jain: None. Background: Mutations of CYP24A1 are known to be associated with hypercalcemia due to disruptions in 24-hydroxylase’s ability to break down 1,25-OH Vitamin D. A case involving heterozygous mutation of CYP24A1 and primary hy...

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Detalles Bibliográficos
Autores principales: Liu, Jannel, Angelos, Peter, Barhoum, Maan, Jain, Rajesh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Bone And Mineral Metabolism
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10553910/
http://dx.doi.org/10.1210/jendso/bvad114.433

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10553910/
http://dx.doi.org/10.1210/jendso/bvad114.433

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