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Results 1 - 10 of 11 for Optic neuropathy
  1. MT-ND1 gene 
    ... ND1 gene are known to cause Leber hereditary optic neuropathy. Each of these mutations changes a single DNA ... 13 percent of all cases of Leber hereditary optic neuropathy. This mutation replaces the nucleotide guanine with the ...
    https://medlineplus.gov/genetics/gene/mt-nd1 - Genetics
  2. MT-ND6 gene 
    ... have been identified in people with Leber hereditary optic neuropathy. This condition is an inherited form of vision ... 14 percent of all cases of Leber hereditary optic neuropathy, and it is the most common cause of ...
    https://medlineplus.gov/genetics/gene/mt-nd6 - Genetics
  3. MT-ND4 gene 
    ... ND4 gene are known to cause Leber hereditary optic neuropathy. This condition is an inherited form of vision ... is the most common cause of Leber hereditary optic neuropathy; it is responsible for about 70 percent of ...
    https://medlineplus.gov/genetics/gene/mt-nd4 - Genetics
  4. MT-ND4L gene 
    ... been identified in several families with Leber hereditary optic neuropathy. This mutation, which can be written as T10663C ... to the vision loss characteristic of Leber hereditary optic neuropathy. This genetic change appears to disrupt the normal ...
    https://medlineplus.gov/genetics/gene/mt-nd4l - Genetics
  5. OPA3 gene 
    ... N, Kitsos G. Mitochondrial Membrane Dynamics and Inherited Optic Neuropathies. In Vivo. 2017 Jul-Aug;31(4):511- ... 304 Chinese Patients with Suspected Childhood-Onset Hereditary Optic Neuropathy. PLoS One. 2017 Jan 12;12(1):e0170090. ...
    https://medlineplus.gov/genetics/gene/opa3 - Genetics
  6. MT-ND5 gene 
    ... characteristic of an eye disease called Leber hereditary optic neuropathy. A few individuals have been reported with signs ... mitochondrial conditions—MELAS, Leigh syndrome, and Leber hereditary optic neuropathy.It is unclear why changes in the MT- ...
    https://medlineplus.gov/genetics/gene/mt-nd5 - Genetics
  7. OPA1 gene 
    ... Molecular screening of 980 cases of suspected hereditary optic neuropathy with a report on 77 novel OPA1 mutations. Hum Mutat. 2009 Jul;30(7):E692-705. doi: 10.1002/humu.21025. Citation on ... in autosomal dominant optic atrophy (ADOA) patients with mutations in the opa1 ...
    https://medlineplus.gov/genetics/gene/opa1 - Genetics
  8. PRPS1 gene 
    ... cause hereditary peripheral neuropathy with hearing loss and optic neuropathy (cmtx5). Am J Hum Genet. 2007 Sep;81( ...
    https://medlineplus.gov/genetics/gene/prps1 - Genetics
  9. WFS1 gene 
    ... Hoefsloot EH, Cruysberg JR, Cremers CW. Autosomal dominant optic neuropathy and sensorineual hearing loss associated with a novel mutation of WFS1. Mol Vis. 2010 Jan 12;16:26-35. Citation on PubMed or Free ... of autosomal dominant optic atrophy and hearing impairment. Am J Med Genet ...
    https://medlineplus.gov/genetics/gene/wfs1 - Genetics
  10. MT-TH gene 
    ... in mitochondrial DNA associated with Leber's hereditary optic neuropathy and cardiomyopathy. J Hum Genet. 2003;48(1): ...
    https://medlineplus.gov/genetics/gene/mt-th - Genetics
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