Jul 2, 2024 · Familial hypocalciuric hypercalcemia (FHH) is a genetic condition characterized by mild hypercalcemia, typically found in otherwise healthy and asymptomatic individuals. …

Nov 1, 2021 · Familial hypocalciuric hypercalcemia (FHH) is an autosomal dominant condition caused by mutations in the calcium sensing receptor gene (CASR). FHH is characterized by …

Familial hypocalciuric hypercalcemia (FHH) is an inherited condition that can cause hypercalcemia, a serum calcium level typically above 10.2 mg/dL; although uncommon. [1] It is …

May 1, 2003 · Familial hypocalciuric hypercalcemia 16 (FHH) is an autosomal-dominant condition with virtually 100 percent penetrance. Most cases are caused by a mutation in the calcium …

Familial hypocalciuric hypercalcemia (FHH) is an inherited disorder that causes abnormally high levels of calcium in the blood (hypercalcemia) and low to moderate levels of calcium in urine …

Jun 25, 2024 · The demonstration that the rare disorder, familial hypocalciuric hypercalcemia (FHH, now called FHH1), was caused by inactivating mutations in the gene for the calcium …

Familial hypocalciuric hypercalcemia (FHH) causes hypercalcemia by three genetic mechanisms: inactivating mutations in the calcium-sensing receptor, the G-protein subunit α11, or adaptor …

Familial hypocalciuric hypercalcemia (HHC) is a heritable disorder of mineral homeostasis that is transmitted as an autosomal dominant trait with a high degree of penetrance.

Dec 9, 2021 · familial hypocalciuric hypercalcemia (FHH) usually presents with hypocalciuria while primary hyperparathrydoidism will present with hypercalciuria no significant symptoms in …

Oct 1, 2010 · Benign familial hypocalciuric hypercalcemia is an autosomal dominant condition characterized by lifelong hypercalcemia, relative hypocalciuria, and inappropriately elevated …