Literature DB >> 7616538

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

S Winata1, I N Arhya, S Moeljopawiro, J T Hinnant, Y Liang, T B Friedman, J H Asher.   

Abstract

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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Year:  1995        PMID: 7616538      PMCID: PMC1050426          DOI: 10.1136/jmg.32.5.336

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  15 in total

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2.  Genetic mapping refines DFNB3 to 17p11.2, suggests multiple alleles of DFNB3, and supports homology to the mouse model shaker-2.

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Journal:  Am J Hum Genet       Date:  1998-04       Impact factor: 11.025

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Journal:  Hum Mutat       Date:  2016-08-21       Impact factor: 4.878

4.  Relaxed Observance of Traditional Marriage Rules Allows Social Connectivity without Loss of Genetic Diversity.

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6.  A novel nonsense mutation in MYO15A is associated with non-syndromic hearing loss: a case report.

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7.  Identification of Novel Candidate Genes and Variants for Hearing Loss and Temporal Bone Anomalies.

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  7 in total

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