Childhood Apraxia of Speech (CAS) is a relatively rare, severe neurodevelopmental motor speech disorder affecting the planning and programming of speech movements.
CAS is present from childhood and can continue across the lifespan. It does not simply disappear with age, although speech can improve substantially with appropriate intervention.
The speech muscles are not necessarily weak or paralysed. The main difficulty is with the brain's ability to plan, programme and sequence the movements needed for accurate and intelligible speech.
CAS is commonly coded under ICD-10 code R48.2, although coding practices can vary between countries and services.
The internationally preferred term is now Childhood Apraxia of Speech (CAS).
Historically, a number of other terms have been used, particularly in the UK.
These include:
The Royal College of Speech and Language Therapists now recommends the term Childhood Apraxia of Speech, in line with international practice.
Some adults who have had CAS since childhood may prefer to describe themselves as having speech apraxia or apraxia of speech, rather than using the word "childhood". Personal preference may therefore differ from the formal diagnostic term. Many adults with CAS dislike this term as they are no longer children and instead prefer speech apraxia or apraxia of speech. Always check the term they feel most comfortable with..
CAS is much less common than speech sound disorders generally.
Speech sound disorders affect a substantial proportion of young children, but CAS represents only a small subgroup.
Published estimates vary because there has historically been inconsistency in diagnostic criteria and terminology.
A commonly cited estimate is around 1 in 1,000 children, although some studies and clinical sources have reported somewhat higher estimates.
CAS has traditionally been reported more often in boys than girls, although both can be affected.
The prevalence may be considerably higher in some specific genetic, neurological and developmental populations.
Because diagnosis can be complex, prevalence figures should always be interpreted cautiously.
For many people with CAS, no single underlying cause is identified.
However, research increasingly suggests that genetics plays an important role.
Recent evidence indicates that up to around one third of children with CAS may have an identifiable genetic cause, including a single-gene change or chromosomal deletion or duplication.
CAS has been associated with a growing number of genetic conditions, including changes involving genes such as:
CAS can also occur more frequently alongside:
Not every child with CAS needs genetic testing, but genetic referral may be considered when CAS occurs alongside broader developmental, neurological or physical features.
CAS can occur alone, but it can also co-occur with other communication and neurodevelopmental conditions.
These may include:
CAS appears to be more common in some groups of autistic people who are minimally verbal or do not use spoken language.
However, evidence suggests that autistic children who are verbal may have CAS at a rate closer to that seen in the wider population.
When CAS co-occurs with another developmental or communication condition, the combined impact may be greater than either condition alone.
This is why assessment should consider the whole communication and developmental profile rather than speech in isolation.
CAS is not only a disorder of early childhood.
Some children make substantial gains with appropriate motor-speech intervention and develop functional spoken communication. However, older children, teenagers and adults may continue to experience difficulties with:
Where treatment has been insufficient, delayed or ineffective, the impact can extend beyond speech into psychosocial, educational and economic areas of life.
CAS also occurs across languages.
It has been documented in speakers of many languages, including:
The core motor-planning difficulty remains the same, but the way CAS presents can vary depending on the sound system, syllable structure, rhythm and stress patterns of the language spoken.
Assessment should therefore take account of the child's full linguistic background and, where possible, examine speech across all languages used.

UK professional guidance on terminology, identification, assessment and management of Childhood Apraxia of Speech.
Helen Stringer, the lead author on this paper is a Friend of Speech Apraxia
https://www.rcslt.org/wp-content/uploads/2024/02/RCSLT-Childhood-Apraxia-of-Speech-CAS-Position-Paper-2024.pd

This document is a free summary of the current evidence on assessment, diagnosis and treatment of Childhood Apraxia of Speech (CAS) from the University of Sydney. The two lead authors Donna Thomas and Tricia McCabe are both Friends of Speech Apraxia.

Professional position statement outlining the definition and recognised characteristics of CAS.
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