Genetic breakthroughs could reshape autism diagnosis in Thailand with early, personalized interventions
A major international study is changing how autism is diagnosed, suggesting more cases may be identified earlier. Researchers from Princeton University and the Simons Foundation report four genetically distinct autism subtypes, offering explanations for cases that previously went unnoticed—especially among girls and individuals with subtler symptoms. Published in Nature Genetics, the study points toward biology-informed screening and the potential for tailored therapies, while addressing stigma for families. The findings resonate in Thailand, where autism awareness and diagnosis remain limited in many regions.
