Hereditary optic atrophy
MONDO:0043878A family of inherited disorders characterized by progressive loss of vision secondary to death of the retinal ganglion cell axons that comprise the optic nerve.
Also known as: hereditary optic atrophy, Atrophies, hereditary optic, atrophy, hereditary optic, hereditary optic Atrophies, optic atrophy, hereditary
26 clinical trials for this condition and its sub-types, 6 tagged with Hereditary optic atrophy itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Hereditary optic atrophy
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Leber hereditary optic neuropathy 18 trials
1 sub-type
- Leber optic atrophy and dystonia 0 trials
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Autosomal dominant optic atrophy 6 trials
6 sub-types
- Autosomal dominant optic atrophy, classic form 3 trials
- Al Gazali Khidr Prem Chandran syndrome 0 trials
- Autosomal dominant optic atrophy and peripheral neuropathy 0 trials
- Autosomal dominant optic atrophy plus syndrome 0 trials Sub-types →
- Optic atrophy 3 0 trials
- Optic atrophy 5 0 trials
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Optic atrophy 6 1 trial
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1 sub-type
- Optic atrophy 9 0 trials
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Optic atrophy 11 0 trials
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Optic atrophy 12 0 trials
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Optic atrophy 14 0 trials
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Optic atrophy 15 0 trials
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Optic atrophy 16 0 trials
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Optic atrophy 2 0 trials
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Optic atrophy 4 0 trials
Most studied deeper sub-types
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Could vitamin B3 save sight in rare genetic blindness?
Disease control Not yet recruitingThis early study tests whether high-dose vitamin B3 (nicotinamide) can help preserve or improve vision in people with Leber's hereditary optic neuropathy (LHON), a rare genetic disease that causes sudden vision loss. Researchers will give 13 participants 2 grams of vitamin B3 dai…
Phase 1 • Sponsor: University Hospital, Angers • Aim: Disease control
Last updated Jun 27, 2026 08:05 UTC
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Are these two eye diseases actually the same? new study aims to find out
Knowledge-focused Not yet recruitingThis study will look back at medical records of 45 people with either Wolfram syndrome or a related eye condition caused by changes in the WFS1 gene. Researchers want to see if these two conditions are truly different by comparing vision loss over time and other health problems. …
Sponsor: Hôpital Necker-Enfants Malades • Aim: Knowledge-focused
Last updated Jun 27, 2026 08:10 UTC