| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 6830875 | Seizure | 2015 | 14 Pages |
Abstract
We present a unique case of refractory mesial temporal lobe epilepsy in siblings, characterized by an identical clinical profile and histopathology of FCD type IIIa, who were successfully treated by epilepsy surgery. The presence of such a high concordance between the clinical and morphological data, together with the occurrence of epilepsy and febrile seizures in three generations of the family pedigree points towards a possible genetic nature of the observed FCD type IIIa.
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Authors
Petr Fabera, Hana Krijtova, Martin Tomasek, David Krysl, Josef Zamecnik, Milan Mohapl, Premysl Jiruska, Petr Marusic,