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The enigma of hyperparathyroidism in hypophosphatemic rickets.

作者信息

Schmitt Claus Peter, Mehls Otto

机构信息

Division of Pediatric Nephrology, University Children's Hospital of Heidelberg, Im Neuenheimer Feld 150, 69120 Heidelberg, Germany.

出版信息

Pediatr Nephrol. 2004 May;19(5):473-7. doi: 10.1007/s00467-004-1443-y. Epub 2004 Mar 11.

Abstract

Familial hypophosphatemic rickets (XLH) is caused by inactivating mutations of the cell surface metalloproteinase PHEX. It is characterized by low-normal serum levels of 1,25-dihydroxyvitamin D(3)[1,25(OH)(2)D(3)], normocalcemia, and hypophosphatemia. Hyperparathyroidism is regularly seen in patients treated with phosphate supplements, although circulating serum phosphate levels do not reach the normal range. The mechanism is unknown. Decreased serum concentrations of ionized calcium following phosphate supplements might contribute to the development of hyperparathyroidism. Secondary and even tertiary hyperparathyroidism can, however, be observed in patients who have never received phosphate treatment. This points to an abnormal regulation of production and/or degradation of parathyroid hormone (PTH). Recently, the expression of the PHEX gene in hypertrophied parathyroid glands of a patient with XLH has been reported. It is unclear whether the mutant PHEX gene can induce hyperparathyroidism by abnormal regulation of peptidases.

摘要

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