(See also Overview of Optic Nerve Disorders.)
Dominant optic atrophy and Leber hereditary optic neuropathy are inherited disorders caused by abnormal genes. Both disorders are uncommon, particularly Leber hereditary optic neuropathy.
Dominant optic atrophy is inherited from the mother or father as a dominant gene, meaning that only one copy of the gene is required for the disorder to develop. In other words, if either the father or the mother has the disease, then each child has a 50% chance of developing it.
Leber hereditary optic neuropathy is inherited through the mother only, because the abnormal genes are located in the mitochondria. Mitochondria are structures in cells that provide energy for the cell and have their own internal genes that are inherited from only the mother. Affected men cannot pass the disease on to their children. Leber hereditary optic neuropathy is more common among males.
In dominant optic atrophy, vision loss begins before the age of 10 years. Some people can also have nystagmus (a rapid jerking movement of the eyes in one direction alternating with a slower drift back to the original position), hearing loss, or both. People also have trouble distinguishing shades of blue and yellow.
In Leber hereditary optic neuropathy, vision loss usually begins between the ages of 15 and 35. Some people have abnormal heart conduction or nervous system function.
There is no effective treatment, but new treatments are being studied. Limiting consumption of alcohol, which may affect the mitochondria, and not using tobacco products may help slow the rate of vision loss.
Magnifiers, large-print devices, and talking watches (low-vision aids) may help people with loss of vision.
Genetic counseling should be considered.
People who have heart or nervous system problems are sent to specialists.