ArticleCureus2025
New Onset of Seizures Leading to the Delayed Diagnosis of Sturge-Weber Syndrome in Adulthood: A Case Report.
Article in Cureus, 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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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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4 authors.
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Abstract
Sturge-Weber syndrome (SWS), also called encephalotrigeminal angiomatosis, is a congenital neurocutaneous disorder. It is characterized by facial and leptomeningeal angiomas as well as neurologic symptoms such as seizures and learning disabilities. We report a case of a 31-year-old male patient who presented with a history consistent with focal seizures. He was found to have a cutaneous angioma (port-wine stain) in the left temporoparietal region. CT brain revealed characteristic curvilinear calcification in the left tempoparietal cortex. The lack of tonic-clonic seizures and the pattern of his port-wine stain may have possibly delayed the diagnosis well into adulthood.
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