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Progression of low-frequency sensorineural hearing loss (DFNA6/14-WFS1).
Pennings RJ, Bom SJ, Cryns K, Flothmann K, Huygen PL, Kremer H, Van Camp G, Cremers CW. Pennings RJ, et al. Arch Otolaryngol Head Neck Surg. 2003 Apr;129(4):421-6. doi: 10.1001/archotol.129.4.421. Arch Otolaryngol Head Neck Surg. 2003. PMID: 12707188
CONCLUSION: Both families showed an autosomal dominant, progressive, low-frequency sensorineural hearing impairment caused by heterozygous WFS1 mutations....
CONCLUSION: Both families showed an autosomal dominant, progressive, low-frequency sensorineural hearing impa …
Inherited sensorineural low-frequency hearing impairment: some aspects of phenotype and epidemiology.
Parving A, Sakihara Y, Christensen B. Parving A, et al. Audiology. 2000 Jan-Feb;39(1):50-60. doi: 10.3109/00206090009073054. Audiology. 2000. PMID: 10749071
This contribution forms part of the HEAR project. It describes some phenotypes of inherited low-frequency sensorineural hearing impairment (LFSHI) and estimates the prevalence of this inherited hearing impairment (HI) based on a clinical series. …
This contribution forms part of the HEAR project. It describes some phenotypes of inherited low-frequency sensorineural …
Autosomal dominant non-syndromal low-frequency sensorineural hearing impairment linked to chromosome 4p16 (DFNA14): statistical analysis of hearing threshold in relation to age and evaluation of vestibulo-ocular functions.
Kunst H, Marres H, Huygen P, Van Camp G, Joosten F, Cremers C. Kunst H, et al. Audiology. 1999 May-Jun;38(3):165-73. doi: 10.3109/00206099909073018. Audiology. 1999. PMID: 10437687 Review.
A Dutch kindred was studied with low-frequency sensorineural hearing impairment linked to a new locus on chromosome 4p16 (DFNA14). ...
A Dutch kindred was studied with low-frequency sensorineural hearing impairment linked to a new locus on …
Two families with phenotypically different hereditary low frequency hearing impairment: longitudinal data and linkage analysis.
Bille M, Munk-Nielsen L, Tranebjaerg L, Parving A. Bille M, et al. Scand Audiol. 2001;30(4):246-54. doi: 10.1080/01050390152704760. Scand Audiol. 2001. PMID: 11845993
Family B was not linked to the region on chromosome 4, further adding to the genetic heterogeneity in low frequency sensorineural hearing impairment....
Family B was not linked to the region on chromosome 4, further adding to the genetic heterogeneity in low frequency sensori …