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XK aprosencephaly

Just diagnosed with XK aprosencephaly?

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

Open the full XK aprosencephaly hub →

Overview

XK aprosencephaly is a rare condition. Also known as Garcia-Lurie syndrome, XK syndrome, XK-aprosencephaly. Tomeko brings together the specialists, research, clinical trials, treatments and community for XK aprosencephaly so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:3469 · OMIM 207770 · ICD-10 Q04.3 · GARD 0000424

Find care for XK aprosencephaly

Authoritative references for XK aprosencephaly

Common questions

I was just diagnosed with XK aprosencephaly — what should I do first?

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

Where can I find a specialist for XK aprosencephaly?

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

Are there clinical trials for XK aprosencephaly?

Tomeko shows live, recruiting studies for XK aprosencephaly 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