Abstract
We report the case of a girl with hemimegalencephaly (HME) and Lennox-Gastaut syndrome (LGS) treated by callosotomy at 1 year of age. Over 10 years, her seizure frequency and severity decreased markedly. Hemispherectomy is the main surgical option for HME although HME appears to correlate with a less favorable seizure outcome. However, the clinical presentation of LGS and possible generalized cortical dysplasia, which is indicative of a secondarily generalized epilepsy, might predict a favorable surgical outcome of corpus callosotomy in patients of HME, as in our case.
| Original language | English |
|---|---|
| Pages (from-to) | 643-646 |
| Number of pages | 4 |
| Journal | Brain and Development |
| Volume | 30 |
| Issue number | 10 |
| DOIs | |
| Publication status | Published - Nov 2008 |
| Externally published | Yes |
Keywords
- Corpus callosotomy
- Epilepsy
- Generalized cortical dysplasia
- Hemimegalencephaly
- Lennox-Gastaut syndrome
ASJC Scopus subject areas
- Pediatrics, Perinatology, and Child Health
- Developmental Neuroscience
- Clinical Neurology
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