Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 31 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 
    ... DEMYELINATING, 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. CASK-related intellectual disability 
    ... intellectual deficit, Najm type Genetic Testing Registry: Syndromic X-linked intellectual disability Najm type National Organization for Rare Disorders (NORD) FG SYNDROME 4; FGS4 INTELLECTUAL DEVELOPMENTAL DISORDER WITH MICROCEPHALY AND PONTINE ...
    https://medlineplus.gov/.../cask-related-intellectual-disability - Genetics
  10. FLNA gene 
    ... A, Auricchio A. Filamin A is mutated in X-linked chronic idiopathic intestinal pseudo-obstruction with central nervous system involvement. Am J Hum Genet. 2007 Apr;80(4):751-8. doi: 10.1086/513321. Epub 2007 ...
    https://medlineplus.gov/genetics/gene/flna - Genetics
previous · 1 · 2 · 3 · 4 · next