Just diagnosed with Familial developmental dysphasia?
You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Familial developmental dysphasia, look for clinical trials, and connect with others living with it — all in one place.
Open the full interactive Familial developmental dysphasia hub →Overview
Familial developmental dysphasia is a rare condition. Also known as Billard-Toutain-Maheut syndrome, FOXP2-associated dysphasia. Tomeko brings together the specialists, research, clinical trials, treatments and community for Familial developmental dysphasia so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:1799 · OMIM 600117 · ICD-10 F80.1 · GARD 0001823
Find care for Familial developmental dysphasia
Authoritative references for Familial developmental dysphasia
Research & market landscape for Familial developmental dysphasia
Following Familial developmental dysphasia for research or industry? Tomeko brings together the recruiting trials, the latest literature, patient organizations, and the specialist and care-center footprint for Familial developmental dysphasia — the real-world landscape behind the condition, in one place.
- Latest Familial developmental dysphasia research on PubMed ↗
- Recruiting Familial developmental dysphasia trials on ClinicalTrials.gov ↗
- Explore the Familial developmental dysphasia 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 Familial developmental dysphasia and every rare condition. See how Tomeko works with industry →
Common questions
What is Familial developmental dysphasia?
Familial developmental dysphasia is a rare condition. Also known as Billard-Toutain-Maheut syndrome, FOXP2-associated dysphasia. For an authoritative medical description see the reference sources on this page; Tomeko brings the specialists, clinical trials, patient organizations and community for Familial developmental dysphasia together in one place.
What are the symptoms of Familial developmental dysphasia?
Symptoms of Familial developmental dysphasia 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 Familial developmental dysphasia.
How is Familial developmental dysphasia treated?
Treatment for Familial developmental dysphasia depends on the individual and is managed by specialists. Use Tomeko to find clinicians and Centers of Excellence who see Familial developmental dysphasia, and review current options with them.
What causes Familial developmental dysphasia — is it genetic?
The cause and inheritance of Familial developmental dysphasia are described in the authoritative references linked on this page. A genetics or specialist clinician who treats Familial developmental dysphasia can explain what it means for you and your family.
I was just diagnosed with Familial developmental dysphasia — what should I do first?
Start by learning the basics from an authoritative source, find a specialist or center that sees Familial developmental dysphasia, and connect with a patient organization. Tomeko brings these together on one hub.
Where can I find a specialist for Familial developmental dysphasia?
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Familial developmental dysphasia, filtered to your area.
Are there clinical trials for Familial developmental dysphasia?
Tomeko shows live, recruiting studies for Familial developmental dysphasia from ClinicalTrials.gov on the hub.
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