Familial developmental dysphasia
Synonyms: Billard-Toutain-Maheut syndrome | FOXP2-associated dysphasia
Familial developmental dysphasia is a severe form of developmental verbal apraxia characterized by a deficit in spontaneous speech writing grammatical judgment and repetition defective articulation moderate to severe degree of dyspraxia a reduced use of consonant clusters and comprehension delay. Hearing and intelligence are normal.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Reference: Access aggregated data from Orphanet at Orphadata.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http: //www.orphadata.org. Data version September 2023.
Newly diagnosed with
Familial developmental dysphasia?
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Advocacy Organizations
Moonshots for Unicorns
Curing single-gene disorders
COMBINEDBrain Inc
COMBINEDBrain is a consortium for outcome measures and biomarkers for neurodevelopmental disorders. We are collaborating to cure rare, non-verbal brain disorders.
Clinical Trials
For a list of clinical trials in this disease area, please click here.