Optic atrophy
MONDO:0003608A disorder characterized by loss of optic nerve fibers. It may be inherited or acquired. Acquired causes include ischemia, optic nerve neuropathy, glaucoma, trauma, radiation, brain tumors, and multiple sclerosis. It leads to vision disturbances.
Also known as: atrophy of optic disk
29 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Leber hereditary optic neuropathy
(17)
Hereditary optic atrophy
(6)
Autosomal dominant optic atrophy
(5)
Autosomal dominant optic atrophy, classic form
(3)
Optic atrophy 6
(1)
ACO2-related optic atrophy with or without extraocular features
(0)
Al Gazali Khidr Prem Chandran syndrome
(0)
Autosomal dominant optic atrophy and peripheral neuropathy
(0)
Autosomal dominant optic atrophy plus syndrome
(0)
Autosomal recessive optic atrophy, OPA7 type
(0)
Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome
(0)
Glaucomatous atrophy of optic disk
(0)
Leber optic atrophy and dystonia
(0)
Optic atrophy 10 with or without ataxia, intellectual disability, and seizures
(0)
Optic atrophy 11
(0)
Optic atrophy 12
(0)
Optic atrophy 13 with retinal and foveal abnormalities
(0)
Optic atrophy 14
(0)
Optic atrophy 15
(0)
Optic atrophy 16
(0)