ORPHA:209908
Isolated childhood apraxia of speech
Also called Isolated CAS, Isolated developmental verbal dyspraxia, Pure CAS, Pure childhood apraxia of speech, Speech and language disorder with orofacial dyspraxia, Speech-language disorder type 1
- Body system
- Neurological diseases
- Inheritance pattern
- Autosomal dominant
- Typical age of onset
- Childhood
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:209908 is classified under "Neurological diseases" in the Orphanet nomenclature.
Common signs
- Delayed speech and language development
- Abnormality of speech or vocalization
- Dysarthria
- Specific learning disability
- Poor speech
- Expressive language delay