Congenital non-syndromal autosomal recessive deafness in Bengkala, an isolated Balinese village.

نویسندگان

  • S Winata
  • I N Arhya
  • S Moeljopawiro
  • J T Hinnant
  • Y Liang
  • T B Friedman
  • J H Asher
چکیده

Bengkala is an Indonesian village located on the north shore of Bali that has existed for over 700 years. Currently, 2.2% of the 2185 people in this village have profound congenital deafness. In response to the high incidence of deafness, the people of Bengkala have developed a village specific sign language which is used by many of the hearing and deaf people. Deafness in Bengkala is congenital, sensorineural, non-syndromal, and caused by a fully penetrant autosomal recessive mutation at the DFNB3 locus. The frequency of the DFNB3 mutation is estimated to be 9.4% among hearing people who have a 17.2% chance of being heterozygous for DFNB3.

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عنوان ژورنال:
  • Journal of medical genetics

دوره 32 5  شماره 

صفحات  -

تاریخ انتشار 1995