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Results 1 - 10 of 27 for Optic neuropathy
  1. Leber hereditary optic neuropathy (LHON) is an inherited form of vision loss. Although this condition usually begins in a person's teens or twenties, rare cases ...
  2. ... 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 ...
  3. ... 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 ...
  4. ... 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 ...
  5. ... 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 ...
  6. ... 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. ...
  7. ... have been identified in people with Leber hereditary optic neuropathy. These genes provide instructions for making proteins that ... oxidative phosphorylation. The mutations responsible for Leber hereditary optic neuropathy change single amino acids in these proteins, which ...
  8. ... 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. ...
  9. ... 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- ...
  10. ... 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 ...
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