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American Focus > Blog > Health and Wellness > Why Autism May Not Be One Condition, But Many
Health and Wellness

Why Autism May Not Be One Condition, But Many

Last updated: July 21, 2025 7:50 am
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Why Autism May Not Be One Condition, But Many
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Autism has long been viewed as a spectrum disorder, with a wide range of traits and characteristics that can vary from mild to severe. However, a recent study published in Nature Genetics has shed new light on the complexity of autism by identifying four distinct subtypes, each with its own genetic timeline, developmental course, and clinical challenges.

The first subtype, labeled as “Social/Behavioral,” consists of children who exhibit typical developmental timelines but display strong autistic traits such as repetitive behaviors and social difficulties. Their genetic profiles reveal common inherited variations, particularly in pathways associated with ADHD and depression.

The second subtype, “Mixed ASD with Developmental Delay,” includes children who experience early struggles with delayed walking, talking, and motor skills. These children carry rare mutations that disrupt the brain’s early development during pregnancy.

The third subtype, “Broadly Affected,” comprises a smaller group of children who face challenges across various domains including language, cognition, and behavior. Their genomes contain significant mutations in genes crucial for early brain formation.

Lastly, the “Moderate Challenges” subtype falls in the middle, displaying subtler disruptions in less essential pathways compared to the other classes.

What sets these subtypes apart is not just the genes that are altered, but when these genetic changes occur. Children in the “Mixed ASD with Developmental Delay” group carry mutations in genes that are expressed during fetal development, shaping the brain’s foundation before the child takes their first steps. In contrast, children in the “Social/Behavioral” group have mutations in genes that activate later, influencing language, emotion, and social understanding postnatally.

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This distinction in timing provides insight into why autism presents differently in each child. By understanding the developmental timelines and brain cell types affected by these genetic mutations, we can gain a deeper appreciation for the complexity of autism.

Moving forward, personalized care for individuals with autism may involve a more nuanced approach that considers the specific biology of each child. As we continue to uncover hidden genetic pathways and refine our understanding of autism, it is essential to recognize the uniqueness of each individual’s experience and provide support that aligns with their specific needs.

In conclusion, autism is not a one-size-fits-all condition but a diverse spectrum of experiences shaped by genetic timelines and developmental processes. By embracing this complexity and tailoring interventions to the individual, we can better support individuals with autism on their unique journey of growth and development.

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