ArticleCureus2024
Isolated Agenesis of the Corpus Callosum in a Four-Year-Old: A Case of Preserved Cognitive Function Despite Complete Corpus Callosum Absence.
Article in Cureus, 2024. 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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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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6 authors.
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Abstract
Agenesis of the corpus callosum (AgCC) is a rare congenital brain anomaly characterized by the partial or complete absence of the corpus callosum, a crucial structure responsible for interhemispheric communication. Neurological outcomes associated with AgCC vary widely, with presentation ranging from severe intellectual disabilities to normal cognitive function. The condition is often discovered incidentally due to the variability in its clinical presentation. This report discusses the case of a four-year-old Saudi boy with incidental AgCC identified following a minor head trauma. The patient was born full-term through spontaneous vaginal delivery without perinatal complications. He presented with a history of mild head trauma leading to recurrent, non-progressive headaches localized in the occipital region. Despite the head trauma, there were no signs of increased intracranial pressure or other neurological deficits. A neurological examination revealed a head circumference above the 95
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