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Results 1 - 4 of 4 for Autosomal dominant nonsyndromic hearing loss 7
  1. Nonsyndromic hearing loss 
    ... TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss. Hum Mutat. 2011 Jul;32(7):825-34. doi: 10.1002/humu.21512. Epub ...
    https://medlineplus.gov/genetics/condition/nonsyndromic-hearing-loss - Genetics
  2. Palmoplantar keratoderma with deafness 
    ... Prera E, Schild C, Aschendorff A, Arndt S. Autosomal dominant prelingual hearing loss with palmoplantar keratoderma syndrome: Variability in clinical expression from mutations of R75W and R75Q in the GJB2 gene. Am J Med Genet A. 2010 Jul;152A(7):1798-802. doi: 10.1002/ajmg.a.33464. ...
    https://medlineplus.gov/.../palmoplantar-keratoderma-with-deafness - Genetics
  3. Stickler syndrome 
    ... gov STICKLER SYNDROME, TYPE I; STL1 ... impairment in Stickler syndrome: a systematic review. Orphanet J Rare Dis. 2012 Oct 30;7:84. doi: 10.1186/1750-1172-7-84. ...
    https://medlineplus.gov/genetics/condition/stickler-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 ...
    https://medlineplus.gov/genetics/condition/retinitis-pigmentosa - Genetics