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Results 1 - 6 of 6 for Infantile sensorineural hearing impairment
  1. BSND gene 
    ... Health Condition MedlinePlus Genetics provides information about Nonsyndromic hearing loss More About This Health Condition BART Bartter syndrome, infantile, with sensorineural deafness (Barttin) barttin barttin CLCNK-type chloride channel ...
    https://medlineplus.gov/genetics/gene/bsnd - Genetics
  2. Infantile-onset spinocerebellar ataxia 
    ... vision loss. Hearing loss caused by nerve damage (sensorineural hearing loss) typically occurs during childhood and progresses to profound ...
    https://medlineplus.gov/.../infantile-onset-spinocerebellar-ataxia - Genetics
  3. Schindler disease 
    ... loss caused by abnormalities of the inner ear (sensorineural hearing loss). They may experience weakness and loss of sensation ...
    https://medlineplus.gov/genetics/condition/schindler-disease - Genetics
  4. CASK-related intellectual disability 
    ... caused by nerve problems in the inner ear (sensorineural hearing loss), and most also have abnormalities affecting the eyes. ...
    https://medlineplus.gov/.../cask-related-intellectual-disability - Genetics
  5. MEGDEL syndrome 
    ... acid.In infancy, individuals with MEGDEL syndrome develop hearing loss caused by changes in the inner ear (sensorineural deafness); the hearing problems gradually worsen over time. ...
    https://medlineplus.gov/genetics/condition/megdel-syndrome - Genetics
  6. SERAC1 gene 
    ... Manov I, Saada A, Sprecher E, Mandel H. Infantile mitochondrial hepatopathy is a cardinal feature of MEGDEL syndrome (3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome) caused by ...
    https://medlineplus.gov/genetics/gene/serac1 - Genetics