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Familial hypocalciuric hypercalcemia caused by homozygous CaSR gene mutation

26 Aug 2020

Abstract excerpt

INTRODUCTION: Familial hypocalciuric hypercalcemia (FHH) is a group of autosomal dominant genetic diseases with persistent hypercalcemia and hypocalciuria. The calcium-sensitive receptor (CaSR) plays an important role in calcium and phosphorus metabolism. PATIENT CONCERNS: A 32-year-old man who had diabetes was admitted to our hospital due to poor glycemic control, and was found to have hypercalcemia,...

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PMID: 32871939
DOI: 10.1097/md.0000000000021940

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