Familial hypocalciuric hypercalcemia
ORPHA:405· ICD-10 E83.5
Definition
Familial hypocalciuric hypercalcemia (FHH) is a generally asymptomatic genetic disorder of phosphocalcic metabolism characterized by lifelong moderate hypercalcemia along with normo- or hypocalciuria and elevated plasma parathyroid hormone (PTH) concentration.
- Prevalence
- Unknown
- Inheritance
- Autosomal dominant
- Age of onset
- All ages