Literature DB >> 22965178

Different mechanisms of intestinal calcium absorption at different life stages: therapeutic implications and long-term responses to treatment in patients with hereditary vitamin D-resistant rickets.

Deepti Chaturvedi1, Michèle Garabedian, Jean-Claude Carel, Juliane Léger.   

Abstract

BACKGROUND: Intestinal calcium absorption is regulated principally by 1,25-dihydroxyvitamin D, but other regulators are also involved. CASE REPORT: The 3 children studied were born with unaffected bones. Two were referred at 21 months of age, with clinical features of severe vitamin D-resistant rickets. They were treated with intravenous calcium for 12-18 months, following an initial lack of response to oral calcium and vitamin D. The third patient, who was exclusively breast-fed, was diagnosed at 4 months of age, due to alopecia. His condition was successfully managed with high doses of oral calcium and vitamin D. All 3 patients were homozygous for a mutation in the DNA-binding domain of vitamin D receptor. At the most recent evaluation of these patients, currently maintained on oral calcium and vitamin D, clinical findings were normal.
CONCLUSION: During gestation, calcium flux across the placenta is normal, preventing bone diseases in affected fetuses. High calcium intake early in life and, perhaps, the maintenance of breastfeeding for several months may constitute an effective approach to ensuring adequate absorption and preventing severe rickets. During childhood, after parenteral calcium treatment to bypass intestinal calcium absorption, it is possible to maintain normal bone through long-term oral calcium supplementation.
Copyright © 2012 S. Karger AG, Basel.

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Year:  2012        PMID: 22965178     DOI: 10.1159/000341405

Source DB:  PubMed          Journal:  Horm Res Paediatr        ISSN: 1663-2818            Impact factor:   2.852


  3 in total

Review 1.  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

2.  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

3.  Hereditary Vitamin D Resistant Rickets: Clinical, Laboratory, and Genetic Characteristics of 2 Iranian Siblings.

Authors:  Ali A Ghazi; Azita Zadeh-Vakili; Marjan Zarif Yeganeh; Shahram Alamdari; Atieh Amouzegar; Ali Akbar Khorsandi; Alireza Amirbaigloo; Fereidoun Azizi
Journal:  Int J Endocrinol Metab       Date:  2017-07-31
  3 in total

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