Medicine
Volume 37, Issue 9 , Pages 465-468, September 2009

Hypocalcaemia

Elaine Murphy MB BCh BAO MRCP (Ire) FRCPath is a locum consultant in Inherited Metabolic Disease at the National Hospital for Neurology and Neurosurgery, London, UK. Competing interests: none declared

Graham R Williams MBBS PhD FRCP is Head of the Molecular Endocrinology Department at Imperial College London and Professor of Endocrinology and Consultant Physician at Hammersmith Hospital, London, UK. Competing interests: none declared

Abstract 

Hypocalcaemia is a frequent condition resulting from inappropriate loss of calcium from the kidneys or gastrointestinal tract. The condition is most commonly a consequence of hypoparathyroidism or vitamin D deficiency. Hypoparathyroidism most commonly occurs following surgical removal of the parathyroid glands, but may result from auto-immune disease, rare inherited disorders of parathyroid hormone synthesis or action, or from infiltrative diseases that compromise parathyroid gland function. Alternatively, metabolic disturbances can result in hypocalcaemia because of disturbance to the normal homeostatic regulation of extracellular calcium concentrations by the physiological interactions between vitamin D, parathyroid hormone and the calcium-sensing receptor. Vitamin D deficiency is common and results primarily from dietary insufficiency or as a result of reduced synthesis of vitamin D precursors in the skin because of reduced exposure to UV radiation. Secondary vitamin D deficiency may be due to malabsorptive disorders of the gastro-intestinal tract, liver failure or chronic renal impairment. The clinical features, diagnosis, causes and treatment of hypocalcaemia will be reviewed in this article.

Keywords: calcium-sensing receptor, Chvostek, hypocalcaemia, hypomagnesaemia, hypoparathyroidism, parathyroid hormone, Trousseau, vitamin D deficiency

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PII: S1357-3039(09)00184-4

doi:10.1016/j.mpmed.2009.06.003

Medicine
Volume 37, Issue 9 , Pages 465-468, September 2009