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Myoclonic epilepsy in infancy

Just diagnosed with Myoclonic epilepsy in infancy?

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

Open the full Myoclonic epilepsy in infancy hub →

Overview

Myoclonic epilepsy in infancy is a rare condition. Also known as Benign myoclonic epilepsy of infancy, Benign myoclonus epilepsy of infancy, MEI. Tomeko brings together the specialists, research, clinical trials, treatments and community for Myoclonic epilepsy in infancy so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:86909 · OMIM 605021, 617976, 618364 · ICD-10 G40.3 · GARD 0019086

Find care for Myoclonic epilepsy in infancy

Authoritative references for Myoclonic epilepsy in infancy

Common questions

I was just diagnosed with Myoclonic epilepsy in infancy — what should I do first?

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

Where can I find a specialist for Myoclonic epilepsy in infancy?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Myoclonic epilepsy in infancy, filtered to your area.

Are there clinical trials for Myoclonic epilepsy in infancy?

Tomeko shows live, recruiting studies for Myoclonic epilepsy in infancy 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