Familial hypocalciuric hypercalcemia diagnostic criteria: Difference between revisions
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==Overview== | ==Overview== | ||
The diagnosis of familial hypocalciuric hypercalcemia is based on | The diagnosis of familial hypocalciuric hypercalcemia is based on the presence of asymptomatic hypercalcemia in the multiple family members, hypercalcemia, and hypocalciuria. | ||
==Diagnostic Criteria== | ==Diagnostic Criteria== | ||
Revision as of 13:01, 22 September 2017
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:
Overview
The diagnosis of familial hypocalciuric hypercalcemia is based on the presence of asymptomatic hypercalcemia in the multiple family members, hypercalcemia, and hypocalciuria.
Diagnostic Criteria
- The diagnosis of FHH is made when the following criteria are met:
- Familial - A genetic condition that runs in multiple family members of the same family
- Hypocalciuric - low urinary calcium
- Hypercalcemia - high serum calcium[1]