Literature DB >> 646734

Dominantly inherited low-frequency hearing loss.

A Parving, N J Johnsen, S Holm-Jensen.   

Abstract

Two families with dominantly inherited low-frequency hearing loss are described. The two families are different in mode of transmission and in audiological findings. On the basis of these two differences, it is claimed that two types of inherited low-frequency hearing loss can be distinguished. One type is the dominantly inherited low-frequency hearing loss with fully penetrant abnormal genes. The other is also most probably due to an autosomal dominant gene, but with incomplete penetrance and probably represents a malformation in the middle ear combined with a defect in the apical part of the cochlear mechanism.

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Year:  1978        PMID: 646734     DOI: 10.3109/00206097809080043

Source DB:  PubMed          Journal:  Audiology        ISSN: 0020-6091


  2 in total

1.  Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss.

Authors:  I N Bespalova; G Van Camp; S J Bom; D J Brown; K Cryns; A T DeWan; A E Erson; K Flothmann; H P Kunst; P Kurnool; T A Sivakumaran; C W Cremers; S M Leal; M Burmeister; M M Lesperance
Journal:  Hum Mol Genet       Date:  2001-10-15       Impact factor: 6.150

2.  Mutations in the Wolfram syndrome type 1 gene (WFS1) define a clinical entity of dominant low-frequency sensorineural hearing loss.

Authors:  Marci M Lesperance; James W Hall; Theresa B San Agustin; Suzanne M Leal
Journal:  Arch Otolaryngol Head Neck Surg       Date:  2003-04
  2 in total

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