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Torsion dystonia 13

Just diagnosed with Torsion dystonia 13?

You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Torsion dystonia 13, look for clinical trials, and connect with others living with it — all in one place.

Open the full Torsion dystonia 13 hub →

Overview

Torsion dystonia 13 is a rare condition. Also known as DYT13, Primary dystonia with mixed phenotype, Primary torsion dystonia with predominant craniocervical or upper limb onset. Tomeko brings together the specialists, research, clinical trials, treatments and community for Torsion dystonia 13 so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:98807 · OMIM 607671 · ICD-10 G24.1 · GARD 0010537

Find care for Torsion dystonia 13

Authoritative references for Torsion dystonia 13

Common questions

I was just diagnosed with Torsion dystonia 13 — what should I do first?

Start by learning the basics from an authoritative source, find a specialist or center that sees Torsion dystonia 13, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for Torsion dystonia 13?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Torsion dystonia 13, filtered to your area.

Are there clinical trials for Torsion dystonia 13?

Tomeko shows live, recruiting studies for Torsion dystonia 13 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