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Results 1 - 10 of 26 for Nonsyndromic Deafness
  1. ... environmental factors, it is not inherited. Isolated deafness Nonsyndromic deafness Nonsyndromic hearing impairment Nonsyndromic hearing loss and deafness ...
  2. ... of 107 diverse families with Usher syndrome and nonsyndromic deafness. Am J Hum Genet. 2002 Aug;71(2): ... Friedman TB, Morell RJ. Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the ...
  3. ... basis of DFNB73: mutations of BSND can cause nonsyndromic deafness or Bartter syndrome. Am J Hum Genet. 2009 ...
  4. ... TBC1D24, a gene associated with epilepsy, also cause nonsyndromic deafness DFNB86. Am J Hum Genet. 2014 Jan 2;94(1):144-52. doi: 10.1016/j.ajhg.2013.12.004. Citation on PubMed or Free ... probable cause for nonsyndromic hearing impairment. Hum Mutat. 2014 Jul;35(7): ...
  5. ... spectrum of MYO7A and evaluation of a novel nonsyndromic deafness DFNB2 allele with residual function. Hum Mutat. 2008 ...
  6. ... other parts of the body. Individuals with DFNA6 nonsyndromic deafness cannot hear low tones (low-frequency sounds), such ...
  7. Enlarged Vestibular Aqueduct (EVA) (Vestibular Disorders Association)  
    Enlarged Vestibular Aqueduct is a condition caused by a malformation in the inner ear that leads to loss of hearing and vestibular function. ... Dizziness ...
  8. ... 27. Citation on PubMed Usami SI, Nishio SY. Nonsyndromic Hearing Loss and Deafness, Mitochondrial. 2004 Oct 22 [updated 2018 Jun 14]. ...
  9. ... NBK1272/ Citation on PubMed Smith RJH, Ranum PT. Nonsyndromic Hearing Loss and Deafness, DFNA3 - RETIRED CHAPTER, FOR HISTORICAL REFERENCE ONLY. 1998 ...
  10. ... 0b013e32830e20b0. Citation on PubMed Smith RJH, Ranum PT. Nonsyndromic Hearing Loss and Deafness, DFNA3 - RETIRED CHAPTER, FOR HISTORICAL REFERENCE ONLY. 1998 ...
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