SAT-361 Familial Hypocalciuric Hypercalcemia Type 3: AP2S1 Mutation

Background: Familial hypocalciuric hypercalcemia (FHH) type 3 can appear similar to primary hyperparathyroidism and make the diagnosis of etiology of hypercalcemia challenging. Clinical Case: A 45-year-old man with hypertension and glaucoma was evaluated in clinic for hypercalcemia. His calcium was...

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Bibliographic Details
Published in:J Endocr Soc
Main Authors: Kerut, Sarah Elizabeth, Cardozo, Licy L Yanes
Format: Artigo
Language:Inglês
Published: Oxford University Press 2020
Subjects:
Bone and Mineral Metabolism
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC7208393/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jendso/bvaa046.337
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