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Results 1 - 5 of 5 for Autosomal recessive nonsyndromic hearing loss 7
  1. Nonsyndromic hearing loss 
    ... P. The role of mitochondrial DNA mutations in hearing loss. Biochem Genet. 2013 Aug;51(7-8):588-602. doi: 10.1007/s10528-013-9589-6. Epub 2013 Apr 21. Citation on PubMed Duman D, Tekin M. Autosomal recessive nonsyndromic deafness genes: a review. Front Biosci (Landmark Ed). ...
    https://medlineplus.gov/genetics/condition/nonsyndromic-hearing-loss - Genetics
  2. Stickler syndrome 
    ... Richards AJ, Martin H, Alexander P, Snead MP. Autosomal Recessive Stickler Syndrome. Genes (Basel). 2022 Jun 24;13(7):1135. doi: 10.3390/genes13071135. Citation on PubMed ...
    https://medlineplus.gov/genetics/condition/stickler-syndrome - Genetics
  3. Deafness-infertility syndrome 
    ... M, Lancet D, Beckmann JS. CATSPER2, a human autosomal nonsyndromic male infertility gene. Eur J Hum Genet. 2003 Jul;11(7):497-502. doi: 10.1038/sj.ejhg.5200991. ...
    https://medlineplus.gov/.../condition/deafness-infertility-syndrome - Genetics
  4. Retinitis pigmentosa 
    ... nonsyndromic. Researchers have identified several major types of nonsyndromic retinitis pigmentosa, which are usually distinguished by their pattern of inheritance: autosomal dominant, autosomal recessive, or X-linked.Less commonly, retinitis pigmentosa occurs ...
    https://medlineplus.gov/genetics/condition/retinitis-pigmentosa - Genetics
  5. Pendred syndrome 
    ... and symptoms. These conditions include a form of nonsyndromic hearing loss (hearing loss ... researchers estimate that it accounts for 7 to 8 percent of all hearing loss that ...
    https://medlineplus.gov/genetics/condition/pendred-syndrome - Genetics