Evidence map›Paper›PMID 41339764›Full record

ReviewChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2025

Long-term cognitive outcomes of Chiari II malformation and corpus callosum abnormalities in myelomeningocele.

Eren Ogut

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Review in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

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1 author.

Eren OgutDepartment of Anatomy, Faculty of Medicine, Istanbul Medeniyet University, Istanbul, 34700, Türkiye. erenogut@yahoo.com.tr.ORCID 0000-0003-2506-9883

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMyelomeningocele (MMC) is a congenital neural tube defect frequently associated with Chiari II malformation and corpus callosum (CC) abnormalities. These structural brain anomalies are suspected to contribute significantly to long-term cognitive impairments, yet their distinct effects remain underexplored. This review seeks to provide a comprehensive evaluation of the literature exploring the relationship between Chiari II malformation, CC abnormalities, and their influence on long-term cognitive outcomes in children and young adults with MMC.

methodsAn electronic search was conducted in PubMed, Embase, Web of Science, and Cochrane Library through May 2025. Studies were included if they assessed cognitive outcomes in individuals with MMC aged ≥ 5 years and reported Chiari II and/or CC anomalies via neuroimaging. A total of 74 studies met the inclusion criteria. Data extraction and quality assessment were performed using the Newcastle-Ottawa Scale. Due to heterogeneity, a narrative synthesis was conducted.

resultsChiari II malformation was consistently associated with deficits in visuospatial skills, executive function, and processing speed. CC abnormalities, particularly splenial and posterior callosal dysgenesis, were linked to impaired interhemispheric transfer and slower cognitive processing. Diffusion Tensor Imaging (DTI) revealed significant microstructural white matter alterations correlated with cognitive scores. Functional Magnetic Resonance Imaging (fMRI) studies demonstrated altered connectivity in default mode and executive networks.

conclusionChiari II and CC anomalies are critical determinants of cognitive outcomes in MMC, independent of hydrocephalus. Longitudinal, multimodal imaging studies are needed to clarify developmental trajectories and support early neuropsychological interventions tailored to structural biomarkers.

Indexed as

Agenesis of Corpus CallosumArnold-Chiari MalformationCognitionCorpus CallosumMeningomyeloceleChildHumansChiari II malformationCognitive outcomesCorpus callosum abnormalitiesDiffusion tensor imagingFunctional MRIMyelomeningocele

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.