Identification of a novel FAM83H mutation and microhardness of an affected molar in autosomal dominant hypocalcified amelogenesis imperfecta

Int Endod J. 2009 Nov;42(11):1039-43. doi: 10.1111/j.1365-2591.2009.01617.x.

Abstract

Aim: To determine the underlying molecular genetic aetiology of a family with the hypocalcified form of amelogenesis imperfecta and to investigate the hardness of the enamel and dentine of a known FAM83H mutation.

Methodology: Mutational screening of the FAM83H on the basis of candidate gene approach was performed. All exons and exon-intron boundaries was amplified and sequenced. A microhardness test was performed to measure the Vickers microhardness value.

Results: A novel nonsense mutation (c.1354C>T, p.Q452X) was identified in the last exon of FAM83H, which resulted in soft, uncalcified enamel. The affected enamel was extremely soft (about 17% of the normal control), but the underlying dentine was as hard as the normal control.

Conclusions: Mutational analysis revealed a novel mutation in FAM83H gene. Hardness of dentine was not affected by the mutation, whilst the enamel was extremely soft.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amelogenesis / genetics*
  • Amelogenesis Imperfecta / genetics*
  • Amelogenesis Imperfecta / pathology
  • Child, Preschool
  • Codon, Nonsense
  • DNA Mutational Analysis
  • Dental Enamel / pathology
  • Dental Enamel Proteins / genetics*
  • Dental Stress Analysis
  • Female
  • Genes, Dominant
  • Hardness
  • Humans
  • Molar / pathology
  • Proteins / genetics*
  • Tooth Calcification / genetics*

Substances

  • Codon, Nonsense
  • Dental Enamel Proteins
  • FAM83H protein, human
  • Proteins