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Autosomal dominant cerebellar ataxia type I

Just diagnosed with Autosomal dominant cerebellar ataxia type I?

You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Autosomal dominant cerebellar ataxia type I, look for clinical trials, and connect with others living with it — all in one place.

Open the full Autosomal dominant cerebellar ataxia type I hub →

Overview

Autosomal dominant cerebellar ataxia type I is a rare condition. Also known as ADCA1, ADCAI, Autosomal dominant cerebellar ataxia type 1, Cerebellar plus syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for Autosomal dominant cerebellar ataxia type I so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:94145 · GARD 0019252

Find care for Autosomal dominant cerebellar ataxia type I

Authoritative references for Autosomal dominant cerebellar ataxia type I

Common questions

I was just diagnosed with Autosomal dominant cerebellar ataxia type I — what should I do first?

Start by learning the basics from an authoritative source, find a specialist or center that sees Autosomal dominant cerebellar ataxia type I, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for Autosomal dominant cerebellar ataxia type I?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Autosomal dominant cerebellar ataxia type I, filtered to your area.

Are there clinical trials for Autosomal dominant cerebellar ataxia type I?

Tomeko shows live, recruiting studies for Autosomal dominant cerebellar ataxia type I from ClinicalTrials.gov on the hub.

Informational only — not medical advice. Always consult a qualified clinician. Provider and reference data from public sources (NIH GARD, Orphanet, OMIM, HPO, MONDO, ClinicalTrials.gov, CMS NPPES). © Tomeko · tomekohealth.com