Literature DB >> 3023230

Hereditary resistance to 1,25-dihydroxyvitamin D: clinical and radiological improvement during high-dose oral calcium therapy.

N Sakati, N J Woodhouse, N Niles, H Harfi, D A de Grange, S Marx.   

Abstract

A 6-year-old boy, of consanguinous parents, presented with severe rickets and alopecia; he was found to have hypocalcaemia and elevated circulating 1,25-dihydroxyvitamin D [1,25-(OH)2D] levels. He showed no calcaemic response to 1,25-(OH)2D3 or ergocalciferol given for 3 or more months in daily doses as high as 48 micrograms and 6 X 10(6) IU, respectively. Analyses with cultured skin fibroblasts revealed a normal capacity and affinity for 1,25-(OH)2D3 in soluble extracts ('cytosol') and in nuclei of intact cells but no detectable response of 25-(OH)D3 24-hydroxylase to 1,25-(OH)2D3 in high concentration. Treatment with high doses of calcium (3-4 g elemental calcium orally per day) produced a striking clinical and radiological improvement. We conclude that high oral doses of calcium can replace many of the actions of calciferols. Therapy with high doses of calcium should be tried in similarly affected cases that appear totally or partially unresponsive to calciferols.

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Year:  1986        PMID: 3023230     DOI: 10.1159/000180568

Source DB:  PubMed          Journal:  Horm Res        ISSN: 0301-0163


  5 in total

Review 1.  Genetic disorders and defects in vitamin d action.

Authors:  Peter J Malloy; David Feldman
Journal:  Endocrinol Metab Clin North Am       Date:  2010-06       Impact factor: 4.741

Review 2.  Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets.

Authors:  David Feldman; Peter J Malloy
Journal:  Bonekey Rep       Date:  2014-03-05

3.  Hereditary vitamin D resistant rickets: identification of a novel splice site mutation in the vitamin D receptor gene and successful treatment with oral calcium therapy.

Authors:  Nina S Ma; Peter J Malloy; Pisit Pitukcheewanont; Daina Dreimane; Mitchell E Geffner; David Feldman
Journal:  Bone       Date:  2009-06-10       Impact factor: 4.398

4.  Detection of Hereditary 1,25-Hydroxyvitamin D-Resistant Rickets Caused by Uniparental Disomy of Chromosome 12 Using Genome-Wide Single Nucleotide Polymorphism Array.

Authors:  Mayuko Tamura; Tsuyoshi Isojima; Minae Kawashima; Hideki Yoshida; Keiko Yamamoto; Taichi Kitaoka; Noriyuki Namba; Akira Oka; Keiichi Ozono; Katsushi Tokunaga; Sachiko Kitanaka
Journal:  PLoS One       Date:  2015-07-08       Impact factor: 3.240

5.  Vitamin D - Dependent Rickets, Type II Case Report.

Authors:  Mehmedali Azemi; Majlinda Berisha; Vlora Ismaili-Jaha; Selim Kolgeci; Rina Hoxha; Violeta Grajçevci-Uka; Teuta Hoxha-Kamberi
Journal:  Mater Sociomed       Date:  2014-02-20
  5 in total

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