Familial Hypocalciuric Hypercalcemia and Neonatal Severe Hyperparathyroidism.
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DOI: 10.1159/000491038
Abstract: Familial hypocalciuric hypercalcemia (FHH) and neonatal severe hyperparathyroidism (NSHPT) are genetically determined variants of primary hyperparathyroidism. FHH usually has a benign course, and patients do not require treatment, whereas NSHPT is a severe disorder often… read more here.
Keywords: hyperparathyroidism; hypocalciuric hypercalcemia; neonatal severe; familial hypocalciuric ... See more keywords
Functional Assessment of Calcium-Sensing Receptor Variants Confirms Familial Hypocalciuric Hypercalcemia
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DOI: 10.1210/jendso/bvac025
Abstract: Abstract Context In the clinic it is important to differentiate primary hyperparathyroidism (PHPT) from the more benign, inherited disorder, familial hypocalciuric hypercalcemia (FHH). Since the conditions may sometimes overlap biochemically, identification of calcium-sensing receptor (CASR)… read more here.
Keywords: hypocalciuric hypercalcemia; functional assessment; sensing receptor; calcium sensing ... See more keywords