Ganglioglioma, Epilepsy, and Intellectual Impairment due to Familial TSC1 Deletion.
Tal GilboaReeval SegelSharon ZeligsonGheona AlterescuHilla Ben-PaziPublished in: Journal of child neurology (2018)
Ganglioglioma may be a phenotypic expression of TSC1. Genetic testing is recommended for infants with brain tumors, especially those with an abnormal familial history.
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