tomeko

Familial developmental dysphasia

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 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

Common questions

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.

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