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Lissencephaly due to LIS1 mutation

Just diagnosed with Lissencephaly due to LIS1 mutation?

You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Lissencephaly due to LIS1 mutation, look for clinical trials, and connect with others living with it — all in one place.

Open the full Lissencephaly due to LIS1 mutation hub →

Overview

Lissencephaly due to LIS1 mutation is a rare condition. Also known as PAFAH1B1-related lissencephaly. Tomeko brings together the specialists, research, clinical trials, treatments and community for Lissencephaly due to LIS1 mutation so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:95232 · OMIM 607432 · ICD-10 Q04.3 · GARD 0016838

Find care for Lissencephaly due to LIS1 mutation

Authoritative references for Lissencephaly due to LIS1 mutation

Common questions

I was just diagnosed with Lissencephaly due to LIS1 mutation — what should I do first?

Start by learning the basics from an authoritative source, find a specialist or center that sees Lissencephaly due to LIS1 mutation, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for Lissencephaly due to LIS1 mutation?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Lissencephaly due to LIS1 mutation, filtered to your area.

Are there clinical trials for Lissencephaly due to LIS1 mutation?

Tomeko shows live, recruiting studies for Lissencephaly due to LIS1 mutation 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