Familial hypocalciuric hypercalcemia diagnostic criteria

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ajay Gade MD[2]]

Overview

The diagnosis of familial hypocalciuric hypercalcemia (FHH) 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:

References

  1. "FHH and Diagnosing FHH. Familial Hypocalciuric Hypercalcemia (FHH); Low Urine Calcium".
  2. Fernández López I, Fernández Peña I, Cózar León MV, Viloria Peñas MM, Martínez De Pinillos Gordillo G, Fernández-Ladreda MT, Duran García S (2011). "[Usefulness of genetic tests in familial hypocalciuric hypercalcemia with atypical clinical presentation]". Endocrinol Nutr (in Spanish; Castilian). 58 (7): 325–30. doi:10.1016/j.endonu.2011.04.004. PMID 21697018.

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