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Results 1 - 10 of 36 for Hearing "loss," "X-linked" 4
  1. Nonsyndromic hearing loss 
    ... KY, Choi JY, Bok J, Kim UK. Nonsyndromic X-linked hearing loss. Front Biosci (Elite Ed). 2012 Jan 1;4(3):924-33. doi: 10.2741/E430. Citation ...
    https://medlineplus.gov/genetics/condition/nonsyndromic-hearing-loss - Genetics
  2. POU3F4 gene 
    ... KY, Choi JY, Bok J, Kim UK. Nonsyndromic X-linked hearing loss. Front Biosci (Elite Ed). 2012 Jan 1;4(3):924-33. doi: 10.2741/E430. Citation ...
    https://medlineplus.gov/genetics/gene/pou3f4 - Genetics
  3. Charcot-Marie-Tooth disease 
    ... DISEASE, TYPE 4A; CMT4A CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 4, WITH OR WITHOUT CEREBELLAR ATAXIA; CMTX4 CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 5; CMTX5 ROUSSY-LEVY HEREDITARY AREFLEXIC DYSTASIA ...
    https://medlineplus.gov/.../condition/charcot-marie-tooth-disease - Genetics
  4. 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
  5. X-linked chondrodysplasia punctata 1 
    ... X-linked chondrodysplasia punctata 1 include delayed development, hearing loss, vision abnormalities, and heart defects. The prevalence of X-linked chondrodysplasia punctata 1 is unknown. Several dozen affected ...
    https://medlineplus.gov/.../x-linked-chondrodysplasia-punctata-1 - Genetics
  6. RPGR gene 
    ... Jablonski MM. Clinical and immunohistochemical evidence for an X linked retinitis pigmentosa syndrome with recurrent infections and hearing loss in association with an RPGR mutation. J Med ...
    https://medlineplus.gov/genetics/gene/rpgr - Genetics
  7. Arts syndrome 
    ... the gene (or genes) for a syndrome with X-linked mental retardation, ataxia, weakness, hearing impairment, loss of vision and a fatal course in early ...
    https://medlineplus.gov/genetics/condition/arts-syndrome - Genetics
  8. Alport syndrome 
    ... but some people experience more severe symptoms. Significant hearing loss, eye abnormalities, and progressive kidney disease are more common in males with the X-linked form of Alport syndrome than in affected females. ...
    https://medlineplus.gov/genetics/condition/alport-syndrome - Genetics
  9. 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
  10. BTK gene 
    ... 12. Citation on PubMed Smith CIE, Berglof A. X-Linked Agammaglobulinemia. 2001 Apr 5 [updated 2016 Aug 4]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews(R) [Internet]. ... database for X-linked agammaglobulinemia. Hum Mutat. 2006 Dec;27(12):1209- ...
    https://medlineplus.gov/genetics/gene/btk - Genetics
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