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Results 1 - 4 of 4 for Autosomal recessive nonsyndromic hearing loss 20
  1. Nonsyndromic hearing loss 
    ... mutations. Usually, each parent of an individual with autosomal recessive hearing loss carries one copy of the mutated gene but does not have hearing loss.Another 20 to 25 percent of nonsyndromic hearing loss has an autosomal dominant pattern of ...
    https://medlineplus.gov/genetics/condition/nonsyndromic-hearing-loss - Genetics
  2. Retinitis pigmentosa 
    ... more than 60 genes are known to cause nonsyndromic retinitis pigmentosa. More ... with the autosomal recessive form of the disorder. The most common of ...
    https://medlineplus.gov/genetics/condition/retinitis-pigmentosa - Genetics
  3. Stickler syndrome 
    ... Van de Heyning P, Usami S. A new autosomal recessive form of Stickler syndrome is caused by a mutation in the COL9A1 gene. Am J Hum Genet. 2006 Sep;79(3):449-57. doi: 10.1086/506478. Epub 2006 Jun 26. Citation on PubMed or Free article on PubMed Central
    https://medlineplus.gov/genetics/condition/stickler-syndrome - Genetics
  4. Perrault syndrome 
    ... this gene affect peroxisome function or lead to hearing loss in affected males and females and ovarian abnormalities in females with Perrault ... This condition is inherited in an autosomal recessive pattern, which means both copies of the gene ...
    https://medlineplus.gov/genetics/condition/perrault-syndrome - Genetics