Epidemiological and genetic studies of congenital profound deafness in the general population of Sichuan, China

Am J Med Genet. 1994 Nov 1;53(2):192-5. doi: 10.1002/ajmg.1320530214.

Abstract

People with congenital profound deafness (CPD) were surveyed in the general population of Sichuan. The prevalence was 0.082% (104/126, 876) of the general population, male 0.086%, female 0.078%. There was no significant difference in prevalence between urban and rural populations. However the population living in the mountains had a much higher prevalence than people from the foothills and plains (P < 0.05). Amongst the nationalities investigated, there were significant differences in prevalence. Non-Chinese, except for Tibetans, presented a significantly higher prevalence than Han Chinese. There was a significantly higher prevalence among the inbred population (0.82%) than among the non-inbred population (0.72%). An effect of parental age was demonstrated, but no effect of birth order was found. There was a significant seasonal variation in prevalence. Inherited cases could account for 71.2% of all cases, of which 92% were autosomal recessive (AR) and 8% autosomal dominant (AD). Heterogeneity in AR was found with at least 8 different loci. The fitness was 60.26%, the coefficient of selection was 0.3974, mutation rate was estimated to be 2.0 x 10(-4), and no heterozygote advantage was proven.

MeSH terms

  • Adolescent
  • Adult
  • Age Distribution
  • Aged
  • Birth Order
  • Child
  • Child, Preschool
  • China / epidemiology
  • Consanguinity
  • Deafness / congenital
  • Deafness / epidemiology*
  • Deafness / genetics
  • Female
  • Gene Frequency
  • Genes, Recessive
  • Heterozygote
  • Humans
  • Infant
  • Infant, Newborn
  • Male
  • Maternal Age
  • Middle Aged
  • Mutation
  • Paternal Age
  • Pedigree
  • Seasons
  • Selection, Genetic