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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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| Publicat a: | J Endocr Soc |
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| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2020
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| Matèries: | |
| Accés en línia: | 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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