A novel missense mutation (C84R) in a patient with type II vitamin d-dependent rickets

Exp Clin Endocrinol Diabetes. 2010 Mar;118(3):177-9. doi: 10.1055/s-0028-1103275. Epub 2010 Feb 9.

Abstract

A 7-year-old boy with severe rickets that by clinical analysis was diagnosed as affected by type II vitamin D-dependent rickets, was evaluated for mutations in the vitamin D receptor gene (VDR). The molecular analysis showed a homozygous state for a novel missense mutation (C84R) in a highly conserved nucleotide in the second Zn finger of the DNA binding domain.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Amino Acid Substitution
  • Child
  • Homozygote
  • Humans
  • Male
  • Molecular Sequence Data
  • Mutation, Missense*
  • Receptors, Calcitriol / genetics*
  • Rickets / genetics*
  • Vitamin D Deficiency / genetics*

Substances

  • Receptors, Calcitriol