You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Infantile-onset autosomal recessive nonprogressive cerebellar ataxia, look for clinical trials, and connect with others living with it — all in one place.
Open the full Infantile-onset autosomal recessive nonprogressive cerebellar ataxia hub →Infantile-onset autosomal recessive nonprogressive cerebellar ataxia is a rare condition. Also known as Autosomal recessive spinocerebellar ataxia type 6, SCAR6. Tomeko brings together the specialists, research, clinical trials, treatments and community for Infantile-onset autosomal recessive nonprogressive cerebellar ataxia so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:284332 · OMIM 608029 · ICD-10 G11.0 · GARD 0004954
Start by learning the basics from an authoritative source, find a specialist or center that sees Infantile-onset autosomal recessive nonprogressive cerebellar ataxia, 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 Infantile-onset autosomal recessive nonprogressive cerebellar ataxia, filtered to your area.
Tomeko shows live, recruiting studies for Infantile-onset autosomal recessive nonprogressive cerebellar ataxia from ClinicalTrials.gov on the hub.