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  2. Kjer's optic neuropathy - Wikipedia

    en.wikipedia.org/wiki/Kjer's_optic_neuropathy

    Vision loss in dominant optic atrophy is due to optic nerve fiber loss from mitochondria dysfunction. Dominant optic atrophy is associated with mutation of the OPA1 gene [9] found on chromosome 3, region q28-qter. Also, 5 other chromosomal genes are described as causing optic atrophy: OPA2 (x-linked), OPA3 (dominant), OPA4 (dominant), OPA5 ...

  3. Optic neuropathy - Wikipedia

    en.wikipedia.org/wiki/Optic_neuropathy

    Dominant optic atrophy is an autosomal dominant disease caused by a defect in the nuclear gene OPA1. A slowly progressive optic neuropathy, dominant optic atrophy, usually presents in the first decade of life and is bilaterally symmetrical.

  4. Wolfram-like syndrome - Wikipedia

    en.wikipedia.org/wiki/Wolfram-like_syndrome

    Individuals with Wolfram-like syndrome usually exhibit early-onset progressive hearing loss which starts around the age of 10 years old, early-onset optic atrophy which usually manifests in a person's mid-teenage–late adulthood years of life, and adult-onset diabetes mellitus.

  5. PEHO syndrome - Wikipedia

    en.wikipedia.org/wiki/PEHO_syndrome

    PEHO syndrome (progressive encephalopathy with edema, hypsarrhythmia and optic atrophy) is an autosomal recessive and dominant, progressive neurodegenerative disorder that starts in the first few weeks or months of life. Early symptoms include infantile spasms, hyparrhythmia, and seizures, and optic atrophy.

  6. Chronic progressive external ophthalmoplegia - Wikipedia

    en.wikipedia.org/wiki/Chronic_progressive...

    Treatments used to treat other pathologies causing ophthalmoplegia has not been shown to be effective. [citation needed] Experimental treatment with tetracycline has been used to improve ocular motility in one patient. [11] Coenzyme Q 10 has also been used to treat this condition. [12] However, most neuro-ophthalmologists do not ascribe to any ...

  7. Wolfram syndrome - Wikipedia

    en.wikipedia.org/wiki/Wolfram_syndrome

    Wolfram syndrome, also called DIDMOAD (diabetes insipidus, diabetes mellitus, optic atrophy, and deafness), is a rare autosomal-recessive genetic disorder that causes childhood-onset diabetes mellitus, optic atrophy, and deafness as well as various other possible disorders including neurodegeneration.

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  9. Non-arteritic anterior ischemic optic neuropathy - Wikipedia

    en.wikipedia.org/wiki/Non-arteritic_anterior...

    Non-arteritic anterior ischemic optic neuropathy (NAION) is a medical condition characterized by loss of vision caused by damage to the optic nerve as a result of ischemia, or insufficient blood supply. The key symptom of NAION is optic disc swelling, which typically resolves within 2 months, but often leads to optic atrophy. The likelihood of ...

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