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Unverricht-Lundborg syndrome

Just diagnosed with Unverricht-Lundborg syndrome?

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

Open the full Unverricht-Lundborg syndrome hub →

Overview

Unverricht-Lundborg syndrome is a rare condition. Also known as EPM1, Progressive myoclonus epilepsy type 1, ULD, Unverricht-Lundborg disease. Tomeko brings together the specialists, research, clinical trials, treatments and community for Unverricht-Lundborg syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:308 · OMIM 254800, 310370, 612437 · ICD-10 G40.3 · GARD 0003876

Find care for Unverricht-Lundborg syndrome

Authoritative references for Unverricht-Lundborg syndrome

Common questions

I was just diagnosed with Unverricht-Lundborg syndrome — what should I do first?

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

Where can I find a specialist for Unverricht-Lundborg syndrome?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Unverricht-Lundborg syndrome, filtered to your area.

Are there clinical trials for Unverricht-Lundborg syndrome?

Tomeko shows live, recruiting studies for Unverricht-Lundborg syndrome 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