A review on the management of epilepsy associated with hypothalamic hamartomas.

Published

Journal Article (Review)

INTRODUCTION: Hypothalamic hamartomas are rare congenital malformations located in the region of the tuber cinereum and third ventricle. Patients may be asymptomatic, but the usual presentation is gelastic seizures, precocious puberty, and/or developmental delay. CLINICAL PRESENTATION: Without surgical intervention, the gelastic seizures, which are typically present in childhood, may progress to other seizure types, including generalized epilepsy, and are generally refractory to antiepileptic drugs. SUMMARY: This review will discuss the clinical and electrophysiologic aspects of these lesions, as well as treatment options, including surgery, endoscopy, and radiosurgery.

Full Text

Duke Authors

Cited Authors

  • Frazier, JL; Goodwin, CR; Ahn, ES; Jallo, GI

Published Date

  • April 2009

Published In

Volume / Issue

  • 25 / 4

Start / End Page

  • 423 - 432

PubMed ID

  • 19153751

Pubmed Central ID

  • 19153751

Electronic International Standard Serial Number (EISSN)

  • 1433-0350

Digital Object Identifier (DOI)

  • 10.1007/s00381-008-0798-y

Language

  • eng

Conference Location

  • Germany