Evidence map›Paper›PMID 41275036›Full record

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

Cranial magnetic resonance imaging findings in 167 patients with spina bifida aperta: a retrospective study.

Gülseli Berivan Sezen, İbrahim Alataş, Hacı Mehmet Saygı, Larisa Andrada Ay, Cenk Çelik, Osman Boyalı

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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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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Gülseli Berivan SezenDepartment of Neurosurgery, Giresun Research and Health Hospital, Giresun, Turkey. berivansezen@gmail.com.
İbrahim AlataşSpina Bifida and Fetal Surgery, Beykent University, Istanbul, Turkey.
Hacı Mehmet SaygıDepartment of Neurosurgery, Beykent University, Istanbul, Turkey.
Larisa Andrada AyDepartment of Neurosurgery, Mardin Kızıltepe State Hospital, Mardin, Turkey.
Cenk ÇelikDepartment of Pediatrics, Beykent University, Istanbul, Turkey.
Osman BoyalıDepartment of Neurosurgery, Gaziosmanpaşa Eğitim Ve Araştırma Hastanesi, Istanbul, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis study aimed to comprehensively evaluate the spectrum and prevalence of cranial magnetic resonance imaging (MRI) findings in a substantial cohort of patients diagnosed with spina bifida aperta. Furthermore, the study sought to contextualize these findings by comparing them with existing literature, thereby contributing to a better understanding of the neurological landscape associated with this common neural tube defect. MATERIALS AND

methodsA retrospective analysis was conducted on the cranial MRI scans of 167 patients who received a diagnosis of spina bifida aperta between January 2022 and December 2024 at Gaziosmanpaşa Research and Training Hospital and İstanbul Demiroglu Bilim University Florance Nightingale Hospital Spina Bifida and Fetal Centre. Demographic data and a detailed assessment of various cranial anomalies, including cerebellar ectopia (Chiari type II malformation), posterior fossa depth, hydrocephalus, tectal beaking, and other less frequent findings, were meticulously recorded and analyzed.

resultsOur analysis revealed a high frequency of cranial anomalies in this patient population. The most prevalent findings were decreased posterior fossa depth (81.4%), cerebellar ectopia consistent with Chiari type II malformation (79.6%), hydrocephalus (69.9%), and tectal beaking (63.5%). Additionally, a range of other cranial abnormalities, including cervicomedullary kink, corpus callosum dysgenesis, and various cortical malformations, were observed with varying frequencies.

conclusionThe significant prevalence of cranial anomalies, particularly those affecting the posterior fossa and ventricular system, underscores the intricate relationship between spinal and intracranial development in spina bifida aperta. Early identification of these anomalies through cranial MRI is crucial for anticipating potential neurological complications, guiding timely interventions, and ultimately optimizing the neurodevelopmental outcomes and long-term care strategies for these patients. This study provides valuable epidemiological data that aligns with and contributes to the existing body of knowledge in the field.

Indexed as

Magnetic Resonance ImagingSpina Bifida CysticaAdolescentAdultArnold-Chiari MalformationChildChild, PreschoolFemaleHumansInfantMaleRetrospective StudiesYoung AdultCerebellar ectopiaChiari type 2Cranial MRIHydrocephalusPosterior fossaSpina bifida apertaTectal beaking

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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.