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Results 1 - 10 of 299 for Hearing impairment
  1. Age-related hearing loss 
    ... so common in the general population. Age-related hearing impairment Deafness due to old age Hearing loss, age-related Old-aged sensorineural hearing impairment Presbyacusia Presbycusis National Organization for Rare Disorders (NORD) ...
    https://medlineplus.gov/genetics/condition/age-related-hearing-loss - Genetics
  2. Nonsyndromic hearing loss 
    ... is not inherited. Isolated deafness Nonsyndromic deafness Nonsyndromic hearing impairment Nonsyndromic hearing loss and deafness Genetic Testing Registry: ...
    https://medlineplus.gov/genetics/condition/nonsyndromic-hearing-loss - Genetics
  3. Pendred syndrome 
    ... and symptoms of the condition. Autosomal recessive sensorineural hearing impairment, enlarged vestibular aqueduct, and goiter Deafness with goiter ...
    https://medlineplus.gov/genetics/condition/pendred-syndrome - Genetics
  4. WFS1 gene 
    ... of the WFS1 gene in Wolfram syndrome, nonsyndromic hearing impairment, diabetes mellitus, and psychiatric disease. Hum Mutat. 2003 ... Tranebjaerg L. Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense ...
    https://medlineplus.gov/genetics/gene/wfs1 - Genetics
  5. Palmoplantar keratoderma with deafness 
    ... is a disorder characterized by skin abnormalities and hearing loss. Affected individuals develop unusually thick skin on the ... of the feet (palmoplantar keratoderma) beginning in childhood. Hearing loss ranges from mild to profound. It begins in ...
    https://medlineplus.gov/.../palmoplantar-keratoderma-with-deafness - Genetics
  6. TECTA gene 
    ... mutations in Iranian families with autosomal recessive nonsyndromic hearing impairment at the DFNB21 locus. Am J Med Genet ... A genotype-phenotype correlation with gender-effect for hearing impairment caused by TECTA mutations. Cell Physiol Biochem. 2004; ...
    https://medlineplus.gov/genetics/gene/tecta - Genetics
  7. STRC gene 
    ... as a major contributor to pediatric bilateral sensorineural hearing impairment. Am J Med Genet A. 2012 Feb;158A( ... T. DFNB16 is a frequent cause of congenital hearing impairment: implementation of STRC mutation analysis in routine diagnostics. ...
    https://medlineplus.gov/genetics/gene/strc - Genetics
  8. Mitochondrial DNA 
    ... T, Schulte-Mattler W, Kornhuber M, Zierz S. Hearing impairment is common in various phenotypes of the mitochondrial ... Central Van Camp G, Smith RJ. Maternally inherited hearing impairment. Clin Genet. 2000 Jun;57(6):409-14. ...
    https://medlineplus.gov/genetics/chromosome/mitochondrial-dna - Genetics
  9. Renal tubular acidosis with deafness 
    ... a disorder characterized by kidney (renal) problems and hearing loss. The kidneys normally filter fluid and waste products ... In people with renal tubular acidosis with deafness, hearing loss caused by changes in the inner ear (sensorineural ...
    https://medlineplus.gov/.../renal-tubular-acidosis-with-deafness - Genetics
  10. Burn-McKeown syndrome 
    ... abnormalities of the nasal passages, characteristic facial features, hearing loss, heart abnormalities, and short stature.In people with ... Some people with Burn-McKeown syndrome have congenital hearing loss in both ears which varies in severity among ...
    https://medlineplus.gov/genetics/condition/burn-mckeown-syndrome - Genetics
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