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Results 1 - 4 of 4 for Optic "atrophy," hearing "loss," peripheral "neuropathy," autosomal dominant
  1. OPA1 gene 
    ... mutations can also cause a condition known as autosomal dominant optic atrophy (ADOA)-plus syndrome. ADOA-plus syndrome involves vision and hearing loss, weakness in the muscles that control eye movement ( ...
    https://medlineplus.gov/genetics/gene/opa1 - Genetics
  2. Charcot-Marie-Tooth disease 
    ... NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIA, WITH OPTIC ATROPHY; HMSN6A ... DOMINANT INTERMEDIATE D; CMTDID CHARCOT-MARIE-TOOTH DISEASE, DOMINANT ...
    https://medlineplus.gov/.../condition/charcot-marie-tooth-disease - Genetics
  3. Spinocerebellar Ataxias Including Machado-Joseph Disease From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Cerebellar Disorders/Specifics ... Cerebellar Disorders ... National Institute of Neurological Disorders and Stroke ... From the National Institutes of Health ... Spinocerebellar ...
    https://www.ninds.nih.gov/...taxias-including-machado-joseph-disease - External Health Links
  4. Leukodystrophy From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Leukodystrophies/Start Here ... Leukodystrophies ... National Institute of Neurological Disorders and Stroke ... From the National Institutes of Health ... Leukodystrophy ...
    https://www.ninds.nih.gov/.../disorders/leukodystrophy - External Health Links