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Non-syndromic, autosomal-recessive deafness.
Petersen MB, Willems PJ. Petersen MB, et al. Clin Genet. 2006 May;69(5):371-92. doi: 10.1111/j.1399-0004.2006.00613.x. Clin Genet. 2006. PMID: 16650073 Review.
The wide range of functions of these DFNB genes reflects the heterogeneity of the genes involved in hearing and hearing loss. Several of these genes are involved in both recessive and dominant deafness, or in both non-syndromic and syndromic deafness. …
The wide range of functions of these DFNB genes reflects the heterogeneity of the genes involved in hearing and hearing los
Features of autosomal recessive non-syndromic hearing impairment: a review to serve as a reference.
Oonk AM, Huygen PL, Kunst HP, Kremer H, Pennings RJ. Oonk AM, et al. Clin Otolaryngol. 2016 Oct;41(5):487-97. doi: 10.1111/coa.12567. Epub 2016 Feb 11. Clin Otolaryngol. 2016. PMID: 26474130 Review.
OBJECTIVE: Non-syndromic sensorineural hearing impairment is inherited in an autosomal recessive fashion in 75-85% of cases. To date, 61 genes with this type of inheritance have been identified as related to hearing impairment, and the genetic h …
OBJECTIVE: Non-syndromic sensorineural hearing impairment is inherited in an autosomal recessive fashion in 75-85
[Genetics of congenital deafness].
Faundes V, Pardo RA, Castillo Taucher S. Faundes V, et al. Med Clin (Barc). 2012 Oct 20;139(10):446-51. doi: 10.1016/j.medcli.2012.02.014. Epub 2012 Apr 24. Med Clin (Barc). 2012. PMID: 22538062 Review. Spanish.
Congenital deafness is defined as the hearing loss which is present at birth and, consequently, before speech development. It is the most prevalent sensor neural disorder in developed countries, and its incidence is estimated between 1-3 children per 1,000 newborns, …
Congenital deafness is defined as the hearing loss which is present at birth and, consequently, before speech development. It …