Literature DB >> 6978889

Circulating vitamin D metabolite levels in hypophosphatasia.

M P Whyte, Y Seino.   

Abstract

25OHD, 1,25,-(OH))2D, and 24,25-(OH)2D were assayed in the serum of 16 patients with the infantile, childhood, or adult form of hypophosphatasia. Except for diminished 1,25-(OH)2D and elevated 24,25-(OH)2D levels in 2 infants (which could be attributed to nonparathyroid hormone-mediated hypercalcemia), the mean circulating level of each vitamin D metabolite was normal in the 3 patient groups. Abnormalities in vitamin D metabolism do not appear to contribute to the pathogenesis of this rare hereditary form of rickets or osteomalacia, which occurs despite normal circulating calcium, inorganic phosphate, and vitamin D metabolite levels.

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Year:  1982        PMID: 6978889     DOI: 10.1210/jcem-55-1-178

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  2 in total

Review 1.  Hypophosphatasia - aetiology, nosology, pathogenesis, diagnosis and treatment.

Authors:  Michael P Whyte
Journal:  Nat Rev Endocrinol       Date:  2016-02-19       Impact factor: 43.330

2.  Reduced bone mineral density and low parathyroid hormone levels in patients with the adult form of hypophosphatasia.

Authors:  C Wüster; R Ziegler
Journal:  Clin Investig       Date:  1992-07
  2 in total

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