FAMILIAL BENIGN HYPERCALCAEMIA: HYPERCALCIURIA AND HYPOCALCIURIA IN AFFECTED MEMBERS OF A SMALL KINDRED
- 1 October 1990
- journal article
- research article
- Published by Wiley in Clinical Endocrinology
- Vol. 33 (4) , 429-433
- https://doi.org/10.1111/j.1365-2265.1990.tb03881.x
Abstract
Familial benign hypercalcaemia has also been termed familial hypocalciuric hypercalcaemia because a major feature of this condition has been a relative hypocalciuria in relation to the hypercalcaemia, such that the calcium to creatinine clearance ratio is less than 0.016. The following is a report of a small kindred of patients with familial benign hypercalcaemia in which two of the affected members have frank hypercalciuria.This publication has 11 references indexed in Scilit:
- A “Carboxyl Terminal” Clinical R Adioim Muno Assay for Parathyroid Hormone with Apparent Recognition Preference for the Intact HormoneJournal of Immunoassay, 1985
- Familial Benign Hypercalcemia (Hypocalciuric Hypercalcemia)Annals of Internal Medicine, 1985
- The Hypocalciuric or Benign Variant of Familial Hypercalcemia: Clinical and Biochemical Features in Fifteen KindredsMedicine, 1981
- The parathyroid glands in familial hypocalciuric hypercalcemiaHuman Pathology, 1981
- The normal parathyroid gland at autopsy: The significance of stromal fat in adult patientsThe Journal of Pathology, 1979
- Circulating Parathyroid Hormone Activity: Familial Hypocalciuric Hypercalcemia Versus Typical Primary Hyperparathyroidism*Journal of Clinical Endocrinology & Metabolism, 1978
- Family studies in patients with primary parathyroid hyperplasiaThe American Journal of Medicine, 1977
- Familial benign hypercalcemiaThe Journal of Pediatrics, 1972