You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities, look for clinical trials, and connect with others living with it — all in one place.
Open the full Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities hub →Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities is a rare condition. Also known as Autosomal recessive childhood-onset dystonia, DYT29 type, Childhood-onset generalized dystonia-optic atrophy syndrome, DYT29, Dystonia 29, Mitochondrial enoyl CoA reductase protein-associated neurodegeneration syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:508093 · OMIM 617282 · ICD-10 G24.1 · GARD 0013488
Start by learning the basics from an authoritative source, find a specialist or center that sees Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities, and connect with a patient organization. Tomeko brings these together on one hub.
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities, filtered to your area.
Tomeko shows live, recruiting studies for Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities from ClinicalTrials.gov on the hub.