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Childhood onset GLUT1 deficiency syndrome 2

Just diagnosed with Childhood onset GLUT1 deficiency syndrome 2?

You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Childhood onset GLUT1 deficiency syndrome 2, look for clinical trials, and connect with others living with it — all in one place.

Open the full Childhood onset GLUT1 deficiency syndrome 2 hub →

Overview

Childhood onset GLUT1 deficiency syndrome 2 is a rare condition. Also known as DYT18, Dystonia 18, PED. Tomeko brings together the specialists, research, clinical trials, treatments and community for Childhood onset GLUT1 deficiency syndrome 2 so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:98811 · OMIM 612126 · ICD-10 G24.8 · GARD 0010541

Find care for Childhood onset GLUT1 deficiency syndrome 2

Authoritative references for Childhood onset GLUT1 deficiency syndrome 2

Common questions

I was just diagnosed with Childhood onset GLUT1 deficiency syndrome 2 — what should I do first?

Start by learning the basics from an authoritative source, find a specialist or center that sees Childhood onset GLUT1 deficiency syndrome 2, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for Childhood onset GLUT1 deficiency syndrome 2?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Childhood onset GLUT1 deficiency syndrome 2, filtered to your area.

Are there clinical trials for Childhood onset GLUT1 deficiency syndrome 2?

Tomeko shows live, recruiting studies for Childhood onset GLUT1 deficiency syndrome 2 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