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Ganglioglioma, Epilepsy, and Intellectual Impairment due to Familial TSC1 Deletion.

Tal GilboaReeval SegelSharon ZeligsonGheona AlterescuHilla Ben-Pazi
Published 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.
Keyphrases
  • early onset
  • poor prognosis
  • binding protein