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Case report of prenatal bilateral cerebellar infarction: implications for social-behavioral functioning
Sara E Whiting1, Audrey M Carson1, Gary D Clark2
1a Psychology Section, Department of Pediatrics , Baylor College of Medicine/Texas Children's Hospital , Houston , TX, USA.
Insights
Prenatal cerebellar infarction can lead to intellectual disability and autism spectrum disorder (ASD). Early injury to the cerebellum may be an acquired pathway for ASD, emphasizing the need for timely, multidisciplinary evaluation.
Area of Science:
- Neuroscience
- Developmental Psychology
- Pediatric Neurology
Background:
- Complete prenatal cerebellar infarction is a rare condition with limited data on developmental outcomes.
- Cerebellar development is crucial for cognitive and social functions.
- Prenatal stroke affecting the cerebellum presents unique challenges in diagnosis and management.
Observation:
- A case study of a child with bilateral cerebellar infarction at 25 weeks gestation.
- Neuropsychological evaluations at ages 5 and 7 years documented intellectual disability and autism spectrum disorder (ASD).
- Social communication deficits were noted, with ASD diagnosis confirmed at age 7.
Findings:
- The child exhibited intellectual disability and confirmed ASD, with minimal developmental progress between ages 5 and 7.
- Early cerebellar injury was associated with significant developmental delays and social deficits.
- Complex medical histories can complicate and delay ASD diagnosis.
Implications:
- The cerebellum plays a critical role in social development, and early injury may be an acquired pathway for ASD.
- Multidisciplinary assessment is vital for early and accurate diagnosis of ASD in children with complex medical conditions.
- This case highlights the cerebellum's involvement in social cognition and potential link to acquired ASD.
Abstract:
Objective: Complete prenatal cerebellar infarction is rare and few reports exist documenting developmental outcomes. We report outcome data on a child who sustained a stroke to the bilateral cerebellar hemispheres at 25 weeks gestation, and was subsequently seen for follow-up neuropsychological evaluations at ages 5 years, 5 months and 7 years, 9 months. Method: Retrospective chart review. Results: Findings from the initial evaluation at age 5 were consistent with a diagnosis of intellectual disability based on developmental testing and parent-reported adaptive behavior. Deficits in social communication, relatedness, and reciprocity were identified, though diagnosis of an autism-spectrum disorder (ASD) was deferred given the difficulty of interpreting these findings in the context of his physical and cognitive disabilities. Re-assessment at age 7 included comprehensive autism assessment, and a diagnosis of ASD was confirmed. Neuropsychological testing revealed minimal developmental skill progression over the assessment interval. Conclusions: These findings add to growing evidence that the cerebellum plays an important role in social development, and that early cerebellar injury may represent an acquired pathway for ASD. Complex medical histories may obscure or delay diagnosis of ASD, highlighting the importance of early evaluation using a multidisciplinary approach.
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