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Cortical tubers, cognition, and epilepsy in tuberous sclerosis. | LitMetric

AI Article Synopsis

  • Tuberous sclerosis complex is an autosomal-dominant disorder causing abnormal growths (hamartomas) in various organs, often leading to high rates of epilepsy and cognitive issues.
  • Our research at the University of Alberta included 24 patients, assessing tuber numbers and locations, seizure types, and cognitive outcomes using imaging and neuropsychological tests.
  • Key findings revealed that more tubers correlate with lower IQ scores, and surgical removal of tubers resulted in freedom from seizures, highlighting the impact of tuber characteristics on cognitive function and seizure management.

Article Abstract

Tuberous sclerosis complex is an autosomal-dominant genetic disorder characterized by hamartomatous growth in various organs. Patients who have this disorder exhibit a high rate of epilepsy and cognitive problems. We investigated number of tubers, location, seizure types, and cognitive outcome, and we analyzed the relationships among them in our tuberous sclerosis patients in the Comprehensive Epilepsy Program at the University of Alberta. We also examined the seizure outcome after tuber resection. Our study cohort included 24 patients with tuberous sclerosis complex. We obtained seizure history, electroencephalogram, and neuropsychologic parameters. Magnetic resonance imaging was used to examine tuber numbers and locations. Ten patients underwent surgical removal of tubers responsible for intractable epilepsy. A negative correlation was found between the number of tubers and intelligent quotient score. Epilepsy surgery led to freedom from seizures in this patient group. We demonstrated that the total number and location of cortical tubers play a significant role in the extent of mental retardation in patients with tuberous sclerosis complex. In addition, patients with intractable seizures and well-defined epileptic focus had excellent surgical outcome.

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Source
http://dx.doi.org/10.1016/j.pediatrneurol.2011.01.001DOI Listing

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