Familial hypocalciuric hypercalcemia diagnostic criteria: Difference between revisions
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**Familial - A genetic condition that runs in multiple family members of the same family | **Familial - A genetic condition that runs in multiple family members of the same family | ||
**Hypocalciuric - low urinary calcium | **Hypocalciuric - low urinary calcium | ||
**Hypercalcemia - high serum calcium | **Hypercalcemia - high serum calcium<ref name="urlFHH and Diagnosing FHH. Familial Hypocalciuric Hypercalcemia (FHH); Low Urine Calcium.">{{cite web |url=http://www.parathyroid.com/FHH.htm |title=FHH and Diagnosing FHH. Familial Hypocalciuric Hypercalcemia (FHH); Low Urine Calcium. |format= |work= |accessdate=}}</ref> | ||
==References== | ==References== | ||
Revision as of 03:44, 22 September 2017
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Familial hypocalciuric hypercalcemia Microchapters |
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Differentiating Familial Hypocalciuric Hypercalcemia from other Diseases |
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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 Familial = As it is a genetic condition it runs in multiple family members. Hypocalciuric = low amount of urinary calcium Hypercalcemia = high serum calcium
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]