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Results 1 - 7 of 7 for Severe sensorineural hearing impairment
  1. PRPS1 gene 
    ... formed from uric acid crystals.People with the severe form of PRS superactivity have additional symptoms including loss of hearing caused by changes in the inner ear (sensorineural hearing loss), weak muscle tone (hypotonia), impaired muscle coordination (ataxia), ...
    https://medlineplus.gov/genetics/gene/prps1 - Genetics
  2. BSND gene 
    ... type IV. This form of the disorder causes severe or life-threatening health ... with sensorineural deafness.BSND gene mutations impair barttin's ability ...
    https://medlineplus.gov/genetics/gene/bsnd - Genetics
  3. WFS1 gene 
    ... WFS1) are a common cause of low frequency sensorineural hearing loss. Hum Mol Genet. 2001 Oct 15;10(22): ... in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutations. Hum Genet. 2002 ...
    https://medlineplus.gov/genetics/gene/wfs1 - Genetics
  4. RRM2B gene 
    ... loss caused by problems with the inner ear (sensorineural hearing loss), and digestive problems.Typically, mutations that cause progressive ...
    https://medlineplus.gov/genetics/gene/rrm2b - Genetics
  5. KCNQ4 gene 
    ... and conductance of the KCNQ4 channel lead to sensorineural hearing loss. J Cell Mol Med. 2013 Jul;17(7): ...
    https://medlineplus.gov/genetics/gene/kcnq4 - Genetics
  6. TECTA gene 
    ... are mutated in each cell. This form of hearing loss is usually severe to profound and is prelingual.The TECTA gene ... results in autosomal dominant, postlingual, progressive, mid frequency hearing ... form of sensorineural pre-lingual non-syndromic deafness, DFNB21. Hum Mol ...
    https://medlineplus.gov/genetics/gene/tecta - Genetics
  7. CLCNKB gene 
    ... syndrome type IV or antenatal Bartter syndrome with sensorineural deafness. In addition to salt wasting, this form of the disorder is characterized by hearing loss that results from a loss of ClC-Ka ...
    https://medlineplus.gov/genetics/gene/clcnkb - Genetics