Transforming growth factor-alpha and nonsyndromic cleft lip with or without palate or cleft palate only in Kelantan, Malaysia

Cleft Palate Craniofac J. 2008 Nov;45(6):583-6. doi: 10.1597/07-020.1. Epub 2008 Jan 6.

Abstract

Objective: To determine the frequency of the transforming growth factor-alpha (TGFalpha) Taq1 polymorphism in nonsyndromic cleft lip with or without cleft palate (CL+/-P) and cleft palate only (CP) in Kelantan, Malaysia.

Setting: The study was conducted at the Combined Cleft Clinic and at the Human Genome Centre in Hospital Universiti Sains Malaysia in Kelantan, Malaysia.

Design: We examined the C2/Taq1 variant of the TGFalpha gene in 46 patients with nonsyndromic CL+/-P or CP only and in 33 controls. The TGFalpha genotype frequencies in patients were compared with those in controls using the chi-square or Fisher exact test. DNA samples were obtained from peripheral blood.

Results: No association was found between TGFalphaTaq1 polymorphism and CL+/-P or CP in this case-control study. In addition, no homozygosity for the rare allele C2 was noted in CL+/-P, CP, or the controls.

Conclusion: No evidence of TGFalphaTaq1 polymorphism was observed in association with CL+/-P and CP in this study.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Case-Control Studies
  • Child
  • Child, Preschool
  • Cleft Lip / genetics*
  • Cleft Palate / genetics*
  • Female
  • Gene Frequency
  • Humans
  • Infant
  • Malaysia
  • Male
  • Polymorphism, Restriction Fragment Length
  • Taq Polymerase / genetics
  • Transforming Growth Factor alpha / genetics*
  • Young Adult

Substances

  • Transforming Growth Factor alpha
  • Taq Polymerase