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Results 1 - 10 of 11 for Profound hearing impairment
  1. GJB2 gene 
    ... hearing loss. It is characterized by mild to profound hearing loss that is present before a child learns to ... after a child learns to speak (postlingual). The hearing loss ranges from mild to profound, becomes more severe over time, and particularly affects ...
    https://medlineplus.gov/genetics/gene/gjb2 - Genetics
  2. MITF gene 
    ... people with Tietz syndrome, which is characterized by profound hearing loss from birth, fair skin, and light-colored hair. ...
    https://medlineplus.gov/genetics/gene/mitf - Genetics
  3. COL11A2 gene 
    ... mutated in each cell. It is characterized by profound hearing loss that is present before a child learns to ...
    https://medlineplus.gov/genetics/gene/col11a2 - Genetics
  4. KCNE1 gene 
    ... that causes an abnormal heart rhythm (arrhythmia) and profound hearing loss from birth. About 10 percent of cases are ...
    https://medlineplus.gov/genetics/gene/kcne1 - Genetics
  5. KCNQ1 gene 
    ... Nielsen syndrome, a condition that causes arrhythmia and profound hearing loss from birth. About 90 percent of cases are ...
    https://medlineplus.gov/genetics/gene/kcnq1 - Genetics
  6. PAX3 gene 
    ... syndrome, a condition characterized by distinctive facial features, profound hearing loss, and abnormalities of the hand muscles that can ...
    https://medlineplus.gov/genetics/gene/pax3 - Genetics
  7. STRC gene 
    ... after a child learns to speak (postlingual). The hearing loss ranges from mild to profound and particularly affects the ability to hear high-frequency sounds.The STRC gene variants that cause nonsyndromic hearing loss add a small amount of DNA to the ...
    https://medlineplus.gov/genetics/gene/strc - Genetics
  8. GJB6 gene 
    ... after a child learns to speak (postlingual). The hearing loss ranges from mild to profound, becomes more severe over time, and particularly affects ...
    https://medlineplus.gov/genetics/gene/gjb6 - Genetics
  9. TECTA gene 
    ... are mutated in each cell. This form of hearing loss is usually severe to profound and is prelingual.The TECTA gene mutations that ...
    https://medlineplus.gov/genetics/gene/tecta - Genetics
  10. CDH23 gene 
    ... hearing loss designated as DFNB12. This type of hearing loss begins before a child learns to speak (prelingual) and is severe to profound.Most of the mutations that cause DFNB12 change ...
    https://medlineplus.gov/genetics/gene/cdh23 - Genetics
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