Modeling childhood epilepsy in brain organoids points to possible treatments
Peer-Reviewed Publication
Updates every hour. Last Updated: 21-Oct-2026 21:17 ET (22-Oct-2026 01:17 GMT/UTC)
When kept alive for more than a year, brain organoids with mutations like those found in the leading cause of childhood epilepsy show developmental anomalies leading to inflammation, pointing to one possible cause of seizures and potential treatments. The disorder, tuberous sclerosis complex, manifests shortly after birth, when potato-shaped lesions form. The organoids develop hyperreactive astrocytes that lead to similar focal lesions. The cells’ gene expression profiles also resemble those seen in neurodegenerative diseases.
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