Just diagnosed with Foix chavany Marie syndrome?
You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Foix chavany Marie syndrome, look for clinical trials, and connect with others living with it — all in one place.
Open the full interactive Foix chavany Marie syndrome hub →Overview
Foix chavany Marie syndrome is a rare condition. Also known as Bilateral anterior opercular syndrome, Facio-pharyngo-glossal diplegia with automatic-voluntary movement dissociation, Facio-pharyngo-glosso-masticatory diplegia. Tomeko brings together the specialists, research, clinical trials, treatments and community for Foix chavany Marie syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:2048 · ICD-10 G12.2 · GARD 0002351
Find care for Foix chavany Marie syndrome
Authoritative references for Foix chavany Marie syndrome
Research & market landscape for Foix chavany Marie syndrome
Following Foix chavany Marie syndrome for research or industry? Tomeko brings together the recruiting trials, the latest literature, patient organizations, and the specialist and care-center footprint for Foix chavany Marie syndrome — the real-world landscape behind the condition, in one place.
- Latest Foix chavany Marie syndrome research on PubMed ↗
- Recruiting Foix chavany Marie syndrome trials on ClinicalTrials.gov ↗
- Explore the Foix chavany Marie syndrome 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 Foix chavany Marie syndrome and every rare condition. See how Tomeko works with industry →
Common questions
What is Foix chavany Marie syndrome?
Foix chavany Marie syndrome is a rare condition. Also known as Bilateral anterior opercular syndrome, Facio-pharyngo-glossal diplegia with automatic-voluntary movement dissociation, Facio-pharyngo-glosso-masticatory diplegia. For an authoritative medical description see the reference sources on this page; Tomeko brings the specialists, clinical trials, patient organizations and community for Foix chavany Marie syndrome together in one place.
What are the symptoms of Foix chavany Marie syndrome?
Symptoms of Foix chavany Marie syndrome 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 Foix chavany Marie syndrome.
How is Foix chavany Marie syndrome treated?
Treatment for Foix chavany Marie syndrome depends on the individual and is managed by specialists. Use Tomeko to find clinicians and Centers of Excellence who see Foix chavany Marie syndrome, and review current options with them.
What causes Foix chavany Marie syndrome — is it genetic?
The cause and inheritance of Foix chavany Marie syndrome are described in the authoritative references linked on this page. A genetics or specialist clinician who treats Foix chavany Marie syndrome can explain what it means for you and your family.
I was just diagnosed with Foix chavany Marie syndrome — what should I do first?
Start by learning the basics from an authoritative source, find a specialist or center that sees Foix chavany Marie syndrome, and connect with a patient organization. Tomeko brings these together on one hub.
Where can I find a specialist for Foix chavany Marie syndrome?
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Foix chavany Marie syndrome, filtered to your area.
Are there clinical trials for Foix chavany Marie syndrome?
Tomeko shows live, recruiting studies for Foix chavany Marie syndrome from ClinicalTrials.gov on the hub.
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