Consanguinity and deafness in Omani children

Int J Audiol. 2008 Jan;47(1):30-3. doi: 10.1080/14992020701703539.

Abstract

This study was based on a national retrospective analysis of 1400 questionnaires on the causes of deafness in Omani children, collected from 1986 to 2000. It was found that 70% of the deaf children were from parents of consanguineous marriages, and 30% from non-consanguineous unions. In those with consanguineous families 70.16% were first cousin marriages, 17.54% were second cousins, and 10.86% were from the same tribe. The proportion arising from first cousin marriages was higher than the background rate of first cousin marriages in Oman. In the total cohort, 45% had other family members with hearing loss. There was a greater chance of other relatives being affected in the consanguineous group as opposed to the non-consanguineous group (29.7% versus 15.3%). In most cases the affected relative was a deaf sibling (67.8%). We have demonstrated a higher rate of consanguinity amongst parents of deaf children in Oman and suggest this is associated with a higher frequency of autosomal recessive deafness in this paediatric population.

MeSH terms

  • Adolescent
  • Child
  • Child, Preschool
  • Cohort Studies
  • Consanguinity*
  • Deafness / epidemiology
  • Deafness / genetics*
  • Female
  • Genes, Recessive*
  • Genetic Predisposition to Disease
  • Humans
  • Infant
  • Male
  • Marriage / statistics & numerical data
  • Oman / epidemiology
  • Pedigree
  • Retrospective Studies
  • Risk Factors
  • Surveys and Questionnaires
  • Time Factors