Gelastic Epilepsy

Author:

Iannetti Paola1,Chessa Luciana2,Raucci Umberto1,Basile Luciano A.1,Fantozzi Luigi M.3,Bozzao Luigi3

Affiliation:

1. Department of Pediatrics, Division of Child Neurology

2. Department of Experimental Medicine, Chair of Medical Genetics

3. Department of Neurologic Science, Chair of Neuroradiology University "La Sapienza" Rome, Italy

Abstract

Gelastic (laughing) epilepsy, relatively uncommon, is usually associated with hypothalamic hamartomas, pituitary tumors, astrocytomas of the mammillary bodies, and dysraphic conditions. Cases of unknown etiology are rare. In three of the four cases reported here, the diagnoses were hamartoma of the tuber cinereum; lobar holoprosencephaly; and lissencephaly type I, grade 2. In the fourth, radiographic investigation gave a normal result; a genetic etiology was suggested because of bilateral familial idiopathic epilepsy. In all patients, EEGs showed both focal spikes and generalized spike-and-wave discharges. The primary underlying neurophysiologic disorder may be provoked by the diffuse hyperexcitability of the cortex and subsequent firing of the thalamocortical networks with which the cortical brain is reciprocally interlinked.

Publisher

SAGE Publications

Subject

Pediatrics, Perinatology and Child Health

Cited by 22 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Hypothalamic Hamartoma;Epilepsy Surgery: A Practical Case-Based Approach;2024

2. Role of NKCC1 and KCC2 in Epilepsy: From Expression to Function;Frontiers in Neurology;2020-01-17

3. Hypothalamic hamartoma;The Treatment of Epilepsy;2015-11-17

4. Rare Combination of Gelastic Epilepsy, Agenesis of the Corpus Callosum, and Hamartoma;Pediatric Neurology;2011-10

5. Functional rundown of gamma-aminobutyric acidA receptors in human hypothalamic hamartomas;Annals of Neurology;2011-03-09

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