NIH GARD Information: MEPAN syndrome
This information is provided by the National Institutes of Health (NIH)
Genetic and Rare Diseases Information Center (GARD).
- Mitochondrial enoyl CoA reductase protein-associated neurodegeneration
- Dystonia, Childhood-Onset, with Optic Atrophy and Basal Ganglia Abnormalities
- Dystonia 20, Childhood-Onset
No overview is available at this time. Please check back for future updates.
For more information, visit GARD.