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 interactive 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
Research & market landscape for XK aprosencephaly
Following XK aprosencephaly for research or industry? Tomeko brings together the recruiting trials, the latest literature, patient organizations, and the specialist and care-center footprint for XK aprosencephaly — the real-world landscape behind the condition, in one place.
- Latest XK aprosencephaly research on PubMed ↗
- Recruiting XK aprosencephaly trials on ClinicalTrials.gov ↗
- Explore the XK aprosencephaly research & specialist footprint on Tomeko
Researchers, patient organizations & industry: Tomeko provides de-identified, no-PHI demand and engagement signal, trial awareness, and a labeled, editorially-firewalled presence for XK aprosencephaly and every rare condition. See how Tomeko works with industry →
Common questions
What is XK aprosencephaly?
XK aprosencephaly is a rare condition. Also known as Garcia-Lurie syndrome, XK syndrome, XK-aprosencephaly. For an authoritative medical description see the reference sources on this page; Tomeko brings the specialists, clinical trials, patient organizations and community for XK aprosencephaly together in one place.
What are the symptoms of XK aprosencephaly?
Symptoms of XK aprosencephaly vary from person to person. For a reviewed, plain-language overview see the authoritative references below (NIH GARD, Orphanet), and discuss your own symptoms with a clinician who treats XK aprosencephaly.
How is XK aprosencephaly treated?
Treatment for XK aprosencephaly depends on the individual and is managed by specialists. Use Tomeko to find clinicians and Centers of Excellence who see XK aprosencephaly, and review current options with them.
What causes XK aprosencephaly — is it genetic?
The cause and inheritance of XK aprosencephaly are described in the authoritative references linked on this page. A genetics or specialist clinician who treats XK aprosencephaly can explain what it means for you and your family.
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.
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