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Assessment and Evaluation of the High Risk Neonate: The NICU Network Neurobehavioral Scale
Published on: August 25, 2014
Early Diagnostics and Early Intervention in Neurodevelopmental Disorders-Age-Dependent Challenges and Opportunities
1University of Groningen, University Medical Center Groningen, Department of Paediatrics-Section Developmental Neurology, 9713 GZ Groningen, The Netherlands.
Insights
Early detection of developmental disorders like cerebral palsy (CP) and autism spectrum disorders (ASD) is possible using specific assessments and understanding brain development milestones. Family involvement is crucial for effective early intervention strategies.
Area of Science:
- Neuroscience
- Developmental Pediatrics
- Child Psychology
Background:
- Developmental disorders require timely diagnosis and intervention for optimal outcomes.
- Brain development, including the dissolution of transient structures like the cortical subplate, influences diagnostic windows.
- Early detection is challenging for conditions like autism spectrum disorders (ASD), with signs often appearing late in the first year.
Purpose of the Study:
- To review current diagnostic tools and intervention strategies for early detection of developmental disorders.
- To correlate diagnostic accuracy with specific brain development stages.
- To emphasize the role of families in early intervention for at-risk infants.
Main Methods:
- Review of literature on early diagnostic instruments for cerebral palsy (CP) and autism spectrum disorders (ASD).
- Analysis of neuroimaging and neurodevelopmental assessment tools (e.g., neonatal MRI, General Movements Assessment, Hammersmith Infant Neurological Examination).
- Examination of predictive value of screening tools (e.g., Modified Checklist for Autism in Toddlers) in relation to brain maturation and familial risk.
Main Results:
- Neonatal MRI, General Movements Assessment, Hammersmith Infant Neurological Examination, and Standardized Infant NeuroDevelopmental Assessment are key for early CP detection.
- Early ASD detection is difficult, but prediction improves with tools like the Modified Checklist for Autism in Toddlers during the second year, especially in high-risk children.
- Diagnostic prediction improves as transient brain structures are replaced by permanent ones, correlating with specific developmental timelines (e.g., cortical subplate dissolution).
Conclusions:
- Effective early diagnosis of developmental disorders relies on a combination of neuroimaging, standardized assessments, and understanding brain development.
- Early intervention is most effective when initiated promptly, with families playing a central role.
- Evidence supports the efficacy of early intervention for medically fragile neonates and infants at various risks for CP and ASD.
Abstract:
This review discusses early diagnostics and early intervention in developmental disorders in the light of brain development. The best instruments for early detection of cerebral palsy (CP) with or without intellectual disability are neonatal magnetic resonance imaging, general movements assessment at 2-4 months and from 2-4 months onwards, the Hammersmith Infant Neurological Examination and Standardized Infant NeuroDevelopmental Assessment. Early detection of autism spectrum disorders (ASD) is difficult; its first signs emerge at the end of the first year. Prediction with the Modified Checklist for Autism in Toddlers and Infant Toddler Checklist is possible to some extent and improves during the second year, especially in children at familial risk of ASD. Thus, prediction improves substantially when transient brain structures have been replaced by permanent circuitries. At around 3 months the cortical subplate has dissolved in primary motor and sensory cortices; around 12 months the cortical subplate in prefrontal and parieto-temporal cortices and cerebellar external granular layer have disappeared. This review stresses that families are pivotal in early intervention. It summarizes evidence on the effectiveness of early intervention in medically fragile neonates, infants at low to moderate risk, infants with or at high risk of CP and with or at high risk of ASD.
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