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Miller Dieker syndrome

Just diagnosed with Miller Dieker syndrome?

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

Open the full Miller Dieker syndrome hub →

Overview

Miller Dieker syndrome is a rare condition. Also known as Lissencephaly due to 17p13.3 deletion, Monosomy 17p13.3, Telomeric deletion 17p. Tomeko brings together the specialists, research, clinical trials, treatments and community for Miller Dieker syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:531 · OMIM 247200 · ICD-10 Q04.3 · GARD 0003669

Find care for Miller Dieker syndrome

Authoritative references for Miller Dieker syndrome

Common questions

I was just diagnosed with Miller Dieker syndrome — what should I do first?

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

Where can I find a specialist for Miller Dieker syndrome?

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

Are there clinical trials for Miller Dieker syndrome?

Tomeko shows live, recruiting studies for Miller Dieker 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