ACO2-related optic atrophy with or without extraocular features

An optic atrophy in which the cause of the disease is monoallelic or biallelic variants in the ACO2 gene. ACO2 is a mitochondrial protein and thus, in addition to the optic atrophy features, features of this disease include abnormal mitochondrial morphology and can affect other organ systems. Extraocular features can include ataxia, spastic paraplegia, CNS abnormalities, neurodevelopmental phenotypes, and retinal degeneration.

Also known as: ACO2-related optic atrophy with or without extraocular features, optic atrophy 9, infantile cerebellar-retinal degeneration

17 clinical trials for this condition and its sub-types, 0 tagged with ACO2-related optic atrophy with or without extraocular features itself.