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Article

Clinical and laboratory features of calcium-sensing receptor disorders: a systematic review.

Annals of clinical biochemistry - 1 Nov 2004

Gunn Ian R, Gaffney Dairena

Abstract excerpt

Mutations in the calcium-sensing receptor gene (CaSR) may result in disorders of calcium homeostasis manifesting as familial benign hypocalciuric hypercalcaemia (FBHH), neonatal severe hyperparathyroidism (NSHPT) or autosomal dominant hypocalcaemia with hypercalciuria (ADHH). FBHH may have a population prevalence as high as one in 16 000, and ADHH one in 70 000. NSHPT is very rare. The FBHH condition is usually...

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Identifiers

PMID: 15588433
DOI: 10.1258/0004563042466802

Genes

PTH

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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