Linkage of autosomal dominant hearing loss to the short ARM of chromosome 1 in two families

Paul Coucke, Guy Van Camp, Bulantrisna Djoyodiharjo, Shelley D Smith, Rune R. Frants, Georges W. Padberg, John K. Darby, Egbert H. Huizing, Cor W R J Cremers, William J. Kimberling, Ben A. Oostra, Paul H. Van De Heyning, Patrick J. Willems

Research output: Contribution to journalArticle

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Abstract

At least half of the cases of profound deafness of early onset are caused by genetic factors, but few of the genetic defects have been identified. This is particularly true of the most common hereditary forms of deafness, which occur in the absence of any associated syndrome. We studied a large Indonesian family in which hearing loss was inherited in an autosomal dominant pattern. The hearing loss first affects the high frequencies during the teens or 20s and becomes profound within 10 years. To locate the responsible gene, we performed genetic-linkage analysis, using microsatellite markers distributed over the entire genome. We then performed linkage analyses in an American family and a Dutch family with similar patterns of hereditary hearing loss. In the extended Indonesian family, a gene linked to deafness mapped to chromosome 1p, with a multipoint lod score of more than 7. In the American family, deafness was linked to the same locus on chromosome 1p, with a multipoint lod score of more than 5. In the Dutch family, however, this locus was ruled out. The flanking markers D1S255 and D1S211 defined a region of 6 cM on chromosome 1p that is likely to contain the gene associated with deafness in the first two families. In some families with early-onset autosomal dominant hearing loss, the responsible gene is on chromosome 1p.

Original languageEnglish (US)
Pages (from-to)425-431
Number of pages7
JournalNew England Journal of Medicine
Volume331
Issue number7
DOIs
StatePublished - Aug 18 1994

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Chromosomes, Human, Pair 1
Hearing Loss
Deafness
Chromosomes
Lod Score
Genes
Genetic Linkage
Microsatellite Repeats
Genome

ASJC Scopus subject areas

  • Medicine(all)

Cite this

Coucke, P., Van Camp, G., Djoyodiharjo, B., Smith, S. D., Frants, R. R., Padberg, G. W., ... Willems, P. J. (1994). Linkage of autosomal dominant hearing loss to the short ARM of chromosome 1 in two families. New England Journal of Medicine, 331(7), 425-431. https://doi.org/10.1056/NEJM199408183310702

Linkage of autosomal dominant hearing loss to the short ARM of chromosome 1 in two families. / Coucke, Paul; Van Camp, Guy; Djoyodiharjo, Bulantrisna; Smith, Shelley D; Frants, Rune R.; Padberg, Georges W.; Darby, John K.; Huizing, Egbert H.; Cremers, Cor W R J; Kimberling, William J.; Oostra, Ben A.; Van De Heyning, Paul H.; Willems, Patrick J.

In: New England Journal of Medicine, Vol. 331, No. 7, 18.08.1994, p. 425-431.

Research output: Contribution to journalArticle

Coucke, P, Van Camp, G, Djoyodiharjo, B, Smith, SD, Frants, RR, Padberg, GW, Darby, JK, Huizing, EH, Cremers, CWRJ, Kimberling, WJ, Oostra, BA, Van De Heyning, PH & Willems, PJ 1994, 'Linkage of autosomal dominant hearing loss to the short ARM of chromosome 1 in two families', New England Journal of Medicine, vol. 331, no. 7, pp. 425-431. https://doi.org/10.1056/NEJM199408183310702
Coucke, Paul ; Van Camp, Guy ; Djoyodiharjo, Bulantrisna ; Smith, Shelley D ; Frants, Rune R. ; Padberg, Georges W. ; Darby, John K. ; Huizing, Egbert H. ; Cremers, Cor W R J ; Kimberling, William J. ; Oostra, Ben A. ; Van De Heyning, Paul H. ; Willems, Patrick J. / Linkage of autosomal dominant hearing loss to the short ARM of chromosome 1 in two families. In: New England Journal of Medicine. 1994 ; Vol. 331, No. 7. pp. 425-431.
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