You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Autosomal recessive DOPA responsive dystonia, look for clinical trials, and connect with others living with it — all in one place.
Open the full Autosomal recessive DOPA responsive dystonia hub →Autosomal recessive DOPA responsive dystonia is a rare condition. Also known as Autosomal recessive Segawa syndrome, DYT5b, Tyrosine hydroxylase deficiency, Tyrosine hydroxylase-deficient dopa-responsive dystonia. Tomeko brings together the specialists, research, clinical trials, treatments and community for Autosomal recessive DOPA responsive dystonia so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:101150 · OMIM 605407, 620453 · ICD-10 G24.1 · GARD 0001902
Start by learning the basics from an authoritative source, find a specialist or center that sees Autosomal recessive DOPA responsive dystonia, 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 Autosomal recessive DOPA responsive dystonia, filtered to your area.
Tomeko shows live, recruiting studies for Autosomal recessive DOPA responsive dystonia from ClinicalTrials.gov on the hub.