Literature DB >> 10968230

Cortical malformations: a frequent cause of epilepsy in children.

L Lagae1.   

Abstract

UNLABELLED: In this review, a simplified scheme for classification of cortical malformations is introduced and illustrated based on the work of Barkovich et al. [8]. Detailed MRI studies identify cortical malformations as a major cause of epilepsy in children. Two aspects that are becoming increasingly important for the paediatrician are emphasised. First, knowledge of the genetic background of cortical malformations is necessary for appropriate genetic counselling. Although the majority of cortical malformations occur sporadically, recent studies have shown a familial pattern in specific epilepsy syndromes associated with cortical malformations. Second, the epilepsy becomes refractory to the common anti-epileptic drugs in many patients with cortical malformations so that epilepsy surgery should be considered. In this respect, the paediatrician can play a pivotal role in referring candidate patients for further specialised assessment.
CONCLUSION: The input of the paediatrician will become crucial to link clinical, genetic and neuro-imaging data in children with the great variety of possible cortical malformations.

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Year:  2000        PMID: 10968230     DOI: 10.1007/s004310000452

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  3 in total

Review 1.  What's new in: "genetics in childhood epilepsy".

Authors:  Lieven Lagae
Journal:  Eur J Pediatr       Date:  2008-03-05       Impact factor: 3.183

2.  Clinical Usefulness of SISCOM-SPM Compared to Visual Analysis to Locate the Epileptogenic Zone.

Authors:  Carla Oliveira Young; Elba C S C Etchbehere; Edna Marina Souza; Sergio Querino Brunetto; Allan de Oliveira Santos; Mariana C L Lima; Sebastian Ortiz-De la Rosa; Marina Alvim; Clarissa Lin Yasuda; Celso Darío Ramos; Fernando Cendes; Barbara Juarez Amorim
Journal:  Front Neurol       Date:  2020-05-29       Impact factor: 4.003

3.  A deletion in Eml1 leads to bilateral subcortical heterotopia in the tish rat.

Authors:  Denise K Grosenbaugh; Suchitra Joshi; Mark P Fitzgerald; Kevin S Lee; Pravin K Wagley; Alexander F Koeppel; Stephen D Turner; Michael J McConnell; Howard P Goodkin
Journal:  Neurobiol Dis       Date:  2020-03-13       Impact factor: 5.996

  3 in total

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