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Results 1 - 10 of 11 for Autosomal recessive nonsyndromic hearing loss 15
  1. Nonsyndromic hearing loss 
    ... pattern. About half of all severe-to-profound autosomal recessive nonsyndromic hearing loss results from mutations in the GJB2 gene; these ... for hearing.The most common cause of moderate autosomal recessive nonsyndromic hearing loss is mutations in the STRC gene. These mutations ...
    https://medlineplus.gov/genetics/condition/nonsyndromic-hearing-loss - Genetics
  2. TECTA gene 
    ... three novel TECTA mutations in Iranian families with autosomal recessive nonsyndromic hearing impairment at the DFNB21 locus. Am J Med Genet A. 2007 Jul 15;143A(14):1623-9. doi: 10.1002/ajmg. ...
    https://medlineplus.gov/genetics/gene/tecta - Genetics
  3. USH2A gene 
    ... mutations are the most common cause of the autosomal recessive form of retinitis pigmentosa, accounting for 10 to 15 percent of all cases. This form of the disorder is described as nonsyndromic, which means that it is not associated with ...
    https://medlineplus.gov/genetics/gene/ush2a - Genetics
  4. GJB3 gene 
    ... pathogenicity of GJB3 and GJB6 variants associated with nonsyndromic hearing loss. ... Non-syndromic, autosomal-recessive deafness. Clin Genet. 2006 May;69(5):371- ...
    https://medlineplus.gov/genetics/gene/gjb3 - Genetics
  5. MYO7A gene 
    ... the inner ear.DFNB2 is inherited in an autosomal recessive pattern, which means both ... hearing loss developed retinitis pigmentosa (a vision disorder ...
    https://medlineplus.gov/genetics/gene/myo7a - Genetics
  6. Deafness-infertility syndrome 
    ... that get interpreted as sound, is responsible for hearing loss. The loss of another gene, CATSPER2, which plays a role in sperm motility, ... syndrome is inherited in an autosomal recessive pattern, which means both copies of chromosome 15 ...
    https://medlineplus.gov/.../condition/deafness-infertility-syndrome - Genetics
  7. STRC gene 
    ... on PubMed Redfield S, Shearer AE. STRC-Related Autosomal Recessive Hearing Loss. 2023 Dec 14. In: Adam MP, Feldman J, ...
    https://medlineplus.gov/genetics/gene/strc - Genetics
  8. About Genetics and Hearing Loss (Centers for Disease Control and Prevention)  
    Hearing Problems in Children/Genetics ... Hearing Problems in Children ... Genes influence a child's risk for having hearing loss in many ways. ... Centers for Disease ...
    https://www.cdc.gov/.../about-genetics-and-hearing-loss.html - External Health Links
  9. Retinitis pigmentosa 
    ... in this gene are responsible for 10 to 15 percent of all cases of autosomal recessive retinitis pigmentosa. Changes in at least six genes ...
    https://medlineplus.gov/genetics/condition/retinitis-pigmentosa - Genetics
  10. Pendred syndrome 
    ... and symptoms. These conditions include a form of nonsyndromic hearing loss (hearing loss that does not affect other parts ... condition. SLC26A4 This condition is inherited in an autosomal recessive pattern, which means both copies of the gene ...
    https://medlineplus.gov/genetics/condition/pendred-syndrome - Genetics
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