אודות פרק זה
Autosomal dominant optic atrophy, or ADOA, is a rare inherited condition that affects the optic nerves and can lead to gradual changes in vision. It is one of at least 350 known types of mitochondrial disease.
In this episode, we explore how ADOA can affect central and colour vision, the role of the OPA1 gene, how the condition can be inherited, and the tests that may be used during diagnosis. We also discuss ADOA plus, where some people may experience additional symptoms affecting hearing, balance, movement, muscles or nerves, as well as ongoing monitoring, support and current research.
The information in this episode is based on Mito Foundation resources. For support, call the Mito Foundation Helpline on 1300 977 180 or visit mito.org.au. Subscribe and follow MitoCast wherever you found this episode.
