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Results 1 - 10 of 22 for Hereditary hearing loss deafness
  1. Nonsyndromic hearing loss 
    ... Testing Registry: X-linked deafness Genetic Testing Registry: Hereditary hearing loss and deafness Nonsyndromic hereditary sensorineural hearing loss National Organization for ...
    https://medlineplus.gov/genetics/condition/nonsyndromic-hearing-loss - Genetics
  2. NIDCD Glossary From the National Institutes of Health (National Institute on Deafness and Other Communication Disorders)  
    Dizziness and Vertigo/Reference Desk ... Dizziness and Vertigo ... Hearing Disorders and Deafness/Reference Desk ... Hearing Disorders and Deafness ... Speech and Communication ...
    https://www.nidcd.nih.gov/glossary - External Health Links
  3. Alport syndrome 
    ... vessels in the kidneys. It can also cause hearing loss and eye problems.
    https://medlineplus.gov/ency/article/000504.htm - Medical Encyclopedia
  4. Palmoplantar keratoderma with deafness 
    ... S. The GJB2 mutation R75Q can cause nonsyndromic hearing loss DFNA3 or hereditary palmoplantar keratoderma with deafness. Am J Med Genet A. 2005 Aug 30; ...
    https://medlineplus.gov/.../palmoplantar-keratoderma-with-deafness - Genetics
  5. Pendred Syndrome From the National Institutes of Health (National Institute on Deafness and Other Communication Disorders)  
    Thyroid Diseases/Related Issues ... Thyroid Diseases ... Hearing Problems in Children/Specifics ... Hearing Problems in Children ... National Institute on Deafness and Other ...
    https://www.nidcd.nih.gov/health/pendred-syndrome - External Health Links
  6. Hereditary sensory and autonomic neuropathy type IE 
    ... their family. DNMT1-complex disorder DNMT1-related dementia, deafness, and sensory neuropathy Hereditary sensory and autonomic neuropathy type 1 with dementia and hearing loss Hereditary sensory neuropathy type IE HSAN1E HSN IE ...
    https://medlineplus.gov/...-sensory-and-autonomic-neuropathy-type-ie - Genetics
  7. Alport syndrome 
    Alport syndrome is a genetic condition characterized by kidney disease, hearing loss, and eye abnormalities.People with Alport syndrome experience progressive ...
    https://medlineplus.gov/genetics/condition/alport-syndrome - Genetics
  8. Deafness is not a burden | NIH MedlinePlus Magazine 
    ... not the same for everyone with the condition. Deafness means partial or complete loss of hearing in one or both ears and can range from mild to severe to profound. It can happen at any age and can be hereditary, genetic, or caused by environmental factors such as ...
    https://magazine.medlineplus.gov/article/deafness-is-not-a-burden - MedlinePlus Magazine
  9. MT-TS1 gene 
    ... Citation on PubMed Usami SI, Nishio SY. Nonsyndromic Hearing Loss and Deafness, Mitochondrial. 2004 Oct 22 [updated 2018 Jun 14]. ...
    https://medlineplus.gov/genetics/gene/mt-ts1 - Genetics
  10. Usher Syndrome From the National Institutes of Health (National Institute on Deafness and Other Communication Disorders)  
    Usher Syndrome/Learn More ... Usher Syndrome ... National Institute on Deafness and Other Communication Disorders ... Usher syndrome is the most common condition that ...
    https://www.nidcd.nih.gov/health/usher-syndrome - External Health Links
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