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Results 1 - 10 of 32 for Hearing "loss," "X-linked" 6
  1. Nonsyndromic hearing loss 
    ... for deafness. Curr Opin Pediatr. 2012 Dec;24(6):679-86. doi: 10.1097/MOP.0b013e3283588f5e. Citation on PubMed or Free article on PubMed Central Song MH, Lee KY, Choi JY, Bok J, Kim UK. Nonsyndromic X-linked hearing loss. Front Biosci (Elite Ed). 2012 Jan 1;4( ...
    https://medlineplus.gov/genetics/condition/nonsyndromic-hearing-loss - Genetics
  2. Newborn Screening Tests for Your Baby (March of Dimes Foundation)  
    Newborn Screening/Specifics ... Newborn Screening ... March of Dimes Foundation
    https://www.marchofdimes.org/.../newborn-screening-tests-your-baby - External Health Links
  3. RPGR gene 
    ... families. Invest Ophthalmol Vis Sci. 2005 Jun;46(6):1891-8. doi: ... infections and hearing loss in association with an RPGR mutation. J Med ...
    https://medlineplus.gov/genetics/gene/rpgr - Genetics
  4. POU3F4 gene 
    ... KY, Choi JY, Bok J, Kim UK. Nonsyndromic X-linked hearing loss. Front Biosci (Elite Ed). 2012 Jan 1;4( ...
    https://medlineplus.gov/genetics/gene/pou3f4 - Genetics
  5. Deafness-dystonia-optic neuronopathy syndrome 
    ... are typically unaffected; however, they may develop mild hearing loss and dystonia. A characteristic of X-linked inheritance is that fathers cannot pass X-linked ...
    https://medlineplus.gov/...ness-dystonia-optic-neuronopathy-syndrome - Genetics
  6. Alport syndrome 
    ... 8. doi: 10.1159/000101802. Epub 2007 Jun 6. Citation on PubMed
    https://medlineplus.gov/genetics/condition/alport-syndrome - Genetics
  7. GJB1 gene 
    ... PubMed Wang Y, Yin F. A Review of X-linked Charcot-Marie-Tooth Disease. J Child Neurol. 2016 May;31(6):761-72. doi: 10.1177/0883073815604227. Epub 2015 ...
    https://medlineplus.gov/genetics/gene/gjb1 - Genetics
  8. Retinitis pigmentosa 
    ... autosomal recessive retinitis pigmentosa. Changes in at least six genes are thought to cause the X-linked form of the disorder. Together, mutations in the ...
    https://medlineplus.gov/genetics/condition/retinitis-pigmentosa - Genetics
  9. Ohdo syndrome, Maat-Kievit-Brunner type 
    ... TG, de Brouwer AP. Mutations in MED12 cause X-linked Ohdo syndrome. Am J Hum Genet. 2013 Mar 7;92(3):401-6. doi: 10.1016/j.ajhg.2013.01.007. ...
    https://medlineplus.gov/.../ohdo-syndrome-maat-kievit-brunner-type - Genetics
  10. Charcot-Marie-Tooth disease 
    ... PubMed Wang Y, Yin F. A Review of X-linked Charcot-Marie-Tooth Disease. J Child Neurol. 2016 May;31(6):761-72. doi: 10.1177/0883073815604227. Epub 2015 ...
    https://medlineplus.gov/.../condition/charcot-marie-tooth-disease - Genetics
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