In a Vietnamese population, MSX1 variants contribute to cleft lip and palate

Genet Med. 2004 May-Jun;6(3):117-25. doi: 10.1097/01.gim.0000127275.52925.05.

Abstract

Purpose: To identify causes of nonsyndromic cleft lip and palate in a Vietnamese population.

Methods: In this study, 175 families with at least one case of cleft lip and/or palate were studied using the candidate genes TGFA, MSX1, and TGFB3.

Results: Transmission distortion for alleles of MSX1 were demonstrated for the whole population and two missense mutations were identified, including one (P147Q) that is found in approximately 2% of the population. The P147Q appears to arise from a founder individual based on shared haplotypes in unrelated families.

Conclusions: MSX1 contributes to nonsyndromic clefting in a Vietnamese population, and consistent with other studies, identifiable mutations in this gene cause about 2% of cases of nonsyndromic clefting.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Alleles*
  • Cleft Lip / genetics*
  • Cleft Palate / genetics*
  • Exons / genetics
  • Family
  • Female
  • Genetic Testing
  • Genetics, Population
  • Haplotypes / genetics*
  • Homeodomain Proteins / genetics*
  • Humans
  • Introns / genetics
  • MSX1 Transcription Factor
  • Male
  • Mutation, Missense / genetics*
  • Pedigree
  • Transforming Growth Factor alpha / genetics
  • Transforming Growth Factor beta / genetics
  • Transforming Growth Factor beta3
  • Vietnam

Substances

  • Homeodomain Proteins
  • MSX1 Transcription Factor
  • MSX1 protein, human
  • Transforming Growth Factor alpha
  • Transforming Growth Factor beta
  • Transforming Growth Factor beta3