A Newly Identified Mutation in the Calcium-Sensing Receptor Gene Causing Familial Hypocalciuric Hypercalcemia: A Case Report
ABSTRACT: Objective: To emphasize the importance of genetic testing of the calcium-sensing receptor (CaSR) in cases where biochemical tests fail to differentiate between primary hyperparathyroidism (PHPT) and familial hypocalciuric hypercalcemia (FHH).Methods: We present the clinical history and lab...
| Main Authors: | , |
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| Format: | Article |
| Language: | English |
| Published: |
Elsevier
2018-11-01
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| Series: | AACE Clinical Case Reports |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S2376060520301334 |