Malformations of cortical development and epilepsy: evaluation of 101 cases (part II)

Malformations of cortical development (MCD) form a spectrum of lesions produced by insult to the developing neocortex. Clinical presentation and electrophysiologic findings of MCD are variable and depend on the affected cortical area. We evaluated epilepsy, EEG, and response to antiepileptic...

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Main Authors: Serdal Güngör, Dilek Yalnizoğlu, Güzide Turanli, Işil Saatçi, Emel Erdoğan-Bakar, Meral Topçu
Format: Article
Language:English
Published: Hacettepe University Institute of Child Health 2007-04-01
Series:The Turkish Journal of Pediatrics
Online Access:https://turkjpediatr.org/article/view/2525
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author Serdal Güngör
Dilek Yalnizoğlu
Güzide Turanli
Işil Saatçi
Emel Erdoğan-Bakar
Meral Topçu
author_facet Serdal Güngör
Dilek Yalnizoğlu
Güzide Turanli
Işil Saatçi
Emel Erdoğan-Bakar
Meral Topçu
author_sort Serdal Güngör
collection DOAJ
description Malformations of cortical development (MCD) form a spectrum of lesions produced by insult to the developing neocortex. Clinical presentation and electrophysiologic findings of MCD are variable and depend on the affected cortical area. We evaluated epilepsy, EEG, and response to antiepileptic treatment in patients with MCD with respect to the neuroimaging findings. We studied 101 patients, ranging between 1 month and 19 years of age. Fifty-four patients were diagnosed with polymicrogyria (PMG), 23 patients with lissencephaly, 12 patients with schizencephaly, and 12 patients with heterotopia. With regards to epilepsy and seizure type, 72/101 (71.3%) patients had epilepsy, and 62/101 (61.4%) patients presented with seizures. Overall, 32.7% of patients had generalized seizures, and 25.7% had complex partial seizures. Mean age at the onset of seizures was 2.7 +/- 3.4 years. The onset of epilepsy tended to be younger in patients with lissencephaly and older in patients with heterotopias. Of the cases, 79.2% had abnormal EEG (56.3% with epileptiform abnormality, 22.9% with non-epileptiform abnormality). EEG was abnormal in 44.9% (13/29) of the cases without epilepsy. EEG showed bilateral synchronous and diffuse epileptiform discharges in 90% of patients with lissencephaly. Patients with schizencephaly had mostly focal epileptiform discharges. Heterotopia cases had a high rate of EEG abnormalities (72.7%). Patients with PMG had epileptiform abnormality in 59.5% of the cases. Patients with heterotopias and PMG achieved better seizure control in comparison with the other groups. In conclusion, epilepsy is the most common problem in MCD. Epilepsy and EEG findings of patients with MCD are variable and seem to be correlated with the extent of cortical involvement.
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spelling doaj-art-96d355290af04eaeafe10135dcdc52c92025-08-20T02:01:57ZengHacettepe University Institute of Child HealthThe Turkish Journal of Pediatrics0041-43012791-64212007-04-01492Malformations of cortical development and epilepsy: evaluation of 101 cases (part II)Serdal Güngör0Dilek YalnizoğluGüzide TuranliIşil SaatçiEmel Erdoğan-BakarMeral TopçuDepartment of Pediatrics, Inönü University, Faculty of Medicine, Malatya, Turkey. Malformations of cortical development (MCD) form a spectrum of lesions produced by insult to the developing neocortex. Clinical presentation and electrophysiologic findings of MCD are variable and depend on the affected cortical area. We evaluated epilepsy, EEG, and response to antiepileptic treatment in patients with MCD with respect to the neuroimaging findings. We studied 101 patients, ranging between 1 month and 19 years of age. Fifty-four patients were diagnosed with polymicrogyria (PMG), 23 patients with lissencephaly, 12 patients with schizencephaly, and 12 patients with heterotopia. With regards to epilepsy and seizure type, 72/101 (71.3%) patients had epilepsy, and 62/101 (61.4%) patients presented with seizures. Overall, 32.7% of patients had generalized seizures, and 25.7% had complex partial seizures. Mean age at the onset of seizures was 2.7 +/- 3.4 years. The onset of epilepsy tended to be younger in patients with lissencephaly and older in patients with heterotopias. Of the cases, 79.2% had abnormal EEG (56.3% with epileptiform abnormality, 22.9% with non-epileptiform abnormality). EEG was abnormal in 44.9% (13/29) of the cases without epilepsy. EEG showed bilateral synchronous and diffuse epileptiform discharges in 90% of patients with lissencephaly. Patients with schizencephaly had mostly focal epileptiform discharges. Heterotopia cases had a high rate of EEG abnormalities (72.7%). Patients with PMG had epileptiform abnormality in 59.5% of the cases. Patients with heterotopias and PMG achieved better seizure control in comparison with the other groups. In conclusion, epilepsy is the most common problem in MCD. Epilepsy and EEG findings of patients with MCD are variable and seem to be correlated with the extent of cortical involvement. https://turkjpediatr.org/article/view/2525
spellingShingle Serdal Güngör
Dilek Yalnizoğlu
Güzide Turanli
Işil Saatçi
Emel Erdoğan-Bakar
Meral Topçu
Malformations of cortical development and epilepsy: evaluation of 101 cases (part II)
The Turkish Journal of Pediatrics
title Malformations of cortical development and epilepsy: evaluation of 101 cases (part II)
title_full Malformations of cortical development and epilepsy: evaluation of 101 cases (part II)
title_fullStr Malformations of cortical development and epilepsy: evaluation of 101 cases (part II)
title_full_unstemmed Malformations of cortical development and epilepsy: evaluation of 101 cases (part II)
title_short Malformations of cortical development and epilepsy: evaluation of 101 cases (part II)
title_sort malformations of cortical development and epilepsy evaluation of 101 cases part ii
url https://turkjpediatr.org/article/view/2525
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