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Results 1 - 10 of 41 for Optic atrophy 15
  1. OPA1 gene 
    ... isoforms expression and apoptosis regulation in autosomal dominant optic atrophy (ADOA) patients with mutations in the opa1 gene. J Neurol Sci. 2015 Apr 15;351(1-2):99-108. doi: 10.1016/ ...
    https://medlineplus.gov/genetics/gene/opa1 - Genetics
  2. Optic atrophy type 1 
    ... isoforms expression and apoptosis regulation in autosomal dominant optic atrophy (ADOA) patients with mutations in the opa1 gene. J Neurol Sci. 2015 Apr 15;351(1-2):99-108. doi: 10.1016/ ...
    https://medlineplus.gov/genetics/condition/optic-atrophy-type-1 - Genetics
  3. Age-related macular degeneration 
    ... in which areas of the macula waste away (atrophy), resulting in severe vision loss. Dry age-related macular degeneration typically affects vision in both eyes, although vision loss often occurs in one eye before the other.In 10 to 15 percent of affected individuals, the dry form progresses ...
    https://medlineplus.gov/.../age-related-macular-degeneration - Genetics
  4. Wolfram syndrome 
    ... the eyes to the brain (a condition called optic atrophy). People with Wolfram syndrome often also have pituitary ... who develops diabetes mellitus requires insulin replacement therapy. Optic atrophy is often the next symptom to appear, usually ...
    https://medlineplus.gov/genetics/condition/wolfram-syndrome - Genetics
  5. MFN2 gene 
    ... carry information from the eyes to the brain (optic atrophy).It is unclear how MFN2 gene mutations lead ... NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIA, WITH OPTIC ATROPHY; HMSN6A MITOFUSIN 2; MFN2 NCBI Gene ClinVar Ando ...
    https://medlineplus.gov/genetics/gene/mfn2 - Genetics
  6. Deafness-dystonia-optic neuronopathy syndrome 
    ... carry information from the eyes to the brain (optic atrophy). Affected individuals can develop an increased sensitivity to ... blindness, dystonia, fractures, and mental deficiency Deafness-dystonia-optic atrophy syndrome Jensen syndrome Mohr-Tranebjærg syndrome Opticoacoustic nerve ...
    https://medlineplus.gov/...ness-dystonia-optic-neuronopathy-syndrome - Genetics
  7. WFS1 gene 
    ... carry information from the eyes to the brain (optic atrophy), and a number of other features involving the ... that is characterized by progressive hearing loss and optic atrophy leading to vision loss, typically beginning in adolescence. ...
    https://medlineplus.gov/genetics/gene/wfs1 - Genetics
  8. Charcot-Marie-Tooth disease 
    ... NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIA, WITH OPTIC ATROPHY; HMSN6A NEUROPATHY, HEREDITARY MOTOR AND SENSORY, RUSSE TYPE; ... NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB, WITH OPTIC ATROPHY; HMSN6B CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2P; ...
    https://medlineplus.gov/.../condition/charcot-marie-tooth-disease - Genetics
  9. Autosomal dominant cerebellar ataxia, deafness, and narcolepsy 
    ... carry information from the eyes to the brain (optic atrophy); clouding of the lenses of the eyes (cataracts); numbness, tingling, or pain in the arms ...
    https://medlineplus.gov/...cerebellar-ataxia-deafness-and-narcolepsy - Genetics
  10. Thiamine-responsive megaloblastic anemia syndrome 
    ... with TRMA have abnormalities of the eye, including optic atrophy, which is the degeneration (atrophy) of the nerves that carry information from the eyes to the brain. Additional features of this condition ...
    https://medlineplus.gov/...-responsive-megaloblastic-anemia-syndrome - Genetics
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