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Autism Spectrum Disorder
GMJ News knowledge hub · last reviewed September 2026 · Georgian Medical Journal
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Autism spectrum disorder (ASD) encompasses a range of neurodevelopmental conditions characterised by differences in social communication, interaction, and patterns of behaviour, interests and activities — affecting an estimated 1 in 100 children globally (approximately 75 million people of all ages), with prevalence rising as diagnostic awareness and criteria improve (WHO). ASD is a spectrum — ranging from non-speaking individuals requiring intensive support to highly capable individuals with subtle differences in social interaction. The neurodiversity framework — recognising autism as a natural variation in human neurology rather than a disorder requiring cure — is reshaping care towards support, inclusion and accommodation rather than normalisation.
Key messages
1 in 100 children globally
Autism spectrum disorder (ASD) affects an estimated 1 in 100 children globally — approximately 75 million people of all ages — though rates vary significantly by methodology; US CDC data suggests approximately 1 in 36 American children (2020) with improved diagnostic detection (WHO).
A spectrum — not a single condition
ASD encompasses a wide range of presentations — from non-speaking individuals requiring intensive support for daily life, to highly capable individuals with subtle differences in social communication and narrow interests. No two autistic people are identical.
Neurodiversity framework
The neurodiversity movement — increasingly influential in research, clinical practice and policy — reframes autism as a natural human variation rather than a disorder to be "cured," emphasising support, accommodation and societal adaptation rather than normalisation.
Early identification improves outcomes
Early identification (before age 2-3 years) allows early intervention — behavioural therapies, speech and language therapy, occupational therapy — that substantially improves communication, social skills and adaptive functioning. Developmental surveillance at every paediatric visit is recommended.
No single cause
ASD has strong genetic underpinnings (approximately 64-91% heritability in twin studies) but no single cause. Hundreds of rare gene mutations and de novo variants contribute; common genetic variants add smaller risks. There is NO causal link between vaccines and autism — extensively studied and refuted.
Substantial unmet support needs
Most autistic people worldwide have no access to diagnosis, support services, education accommodations or mental health care. In LMICs, autism is rarely recognised or diagnosed. Stigma, social exclusion and abuse are major concerns.
Key statistics
Autism diagnosis rates per 1,000 children in selected countries — WHO/national data
Source: Rates reflect diagnostic infrastructure and awareness — not necessarily true prevalence differences.
Glossary of key terms
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About this hub. Produced by the GMJ News Editorial Team as a public-good service. Every statistic is linked to its primary source. Documents are preserved in the GMJ Repository with full attribution. Georgian Medical Journal · Contact the editorial team

