Mutations in the Ca2+-sensing receptor gene cause autosomal dominant and sporadic hypoparathyroidism

Jeffrey Baron*, Karen K. Winer, Jack A. Yanovski, Adrienne W. Cunningham, Louisa Laue, Donald Zimmerman, Gordon B. Cutler

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

174 Scopus citations


Parathyroid hormone secretion is negatively regulated by a 7-transmembrane domain, G-protein coupled Ca2+-sensing receptor. We hypothesized that activating mutations in this receptor might cause autosomal dominant hypoparathyroidism (ADHP). Consistent with this hypothesis, we identified, in two families with ADHP, heterozygous missense mutations in the Ca2+-sensing receptor gene that cosegregated with the disorder. None of 50 normal controls had either mutation. We also identified a de nova, missense Ca2+-sensing receptor mutation in a child with severe sporadic hypoparathyroidism. The amino acid substitution in one ADHP family affected the N-terminal, extracellular domain of the receptor. The other mutations involved the transmembrane region. Unlike patients with acquired hypoparathyroidism, patients with these mutations had hypercalciuria even at low serum calcium concentrations. Their greater hypercalciuria presumably reflected activation of Ca2+-sensing receptors in kidney cells, where the receptor negatively regulates calcium reabsorption. This augmented hypercalciuria increases the risk of renal complications and thus has implications for the choice of therapy.

Original languageEnglish (US)
Pages (from-to)601-606
Number of pages6
JournalHuman molecular genetics
Issue number5
StatePublished - May 1996

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Genetics(clinical)


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