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 - 7 of 7 for Childhood onset sensorineural hearing impairment
  1. Deafness-dystonia-optic neuronopathy syndrome 
    ... caused by nerve damage in the inner ear (sensorineural hearing loss), which ... the onset of these symptoms varies among affected individuals. Some ...
    https://medlineplus.gov/...ness-dystonia-optic-neuronopathy-syndrome - Genetics
  2. ATP1A3 gene 
    ... the movement abnormalities seen in people with rapid-onset dystonia parkinsonism. ... in infancy or early childhood during or following an illness that causes a ...
    https://medlineplus.gov/genetics/gene/atp1a3 - Genetics
  3. Bartter syndrome 
    ... weakness, cramping, and fatigue. Rarely, affected children develop hearing loss ... form, begins in early childhood and tends to be less severe. Once the ...
    https://medlineplus.gov/genetics/condition/bartter-syndrome - Genetics
  4. Infantile-onset spinocerebellar ataxia 
    ... vision loss. Hearing loss caused by nerve damage (sensorineural hearing loss) typically occurs during childhood and progresses to profound deafness.Individuals with IOSCA ...
    https://medlineplus.gov/.../infantile-onset-spinocerebellar-ataxia - Genetics
  5. TK2-related mitochondrial DNA depletion syndrome, myopathic form 
    ... caused by nerve damage in the inner ear (sensorineural hearing loss) may ... childhood. Rarely, the disorder progresses slowly and affected individuals ...
    https://medlineplus.gov/...ial-dna-depletion-syndrome-myopathic-form - Genetics
  6. Riboflavin transporter deficiency neuronopathy 
    ... caused by nerve damage in the inner ear (sensorineural hearing loss) and signs of damage to other nerves.In ... the condition begins in children or young adults, sensorineural hearing loss usually occurs first, followed by signs of pontobulbar ...
    https://medlineplus.gov/...lavin-transporter-deficiency-neuronopathy - Genetics
  7. Autosomal dominant optic atrophy and cataract 
    ... and LHON in 304 Chinese Patients with Suspected Childhood-Onset Hereditary Optic Neuropathy. PLoS One. 2017 Jan 12; ...
    https://medlineplus.gov/...somal-dominant-optic-atrophy-and-cataract - Genetics