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Genetic and forensic implications in epilepsy and cardiac arrhythmias: a case series

Partemi, Sara and Coll Vidal, Monica and Striano, Pasquale and Campuzano, Oscar and Allegue, Catarina and Pezzella, Marianna and Elia, Maurizio and Parisi, Pasquale and Belcastro, Vincenzo and Casellato, Susanna and Giordano, Lucio and Mastrangelo, Massimo and Pietrafusa, Nicola and Striano, Salvatore and Zara, Federico and Bianchi, Amedeo and Buti, Daniela and La Neve, Angela and Tassinari, Carlo Alberto and Oliva, Antonio and Brugada, Ramon (2015) Genetic and forensic implications in epilepsy and cardiac arrhythmias: a case series. International Journal of Legal Medicine, Vol. 129 (3), p. 495-504. ISSN 0937-9827. eISSN 1437-1596. Article.

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DOI: 10.1007/s00414-014-1063-4


Epilepsy affects approximately 3 % of the world’s population, and sudden death is a significant cause of death in this population. Sudden unexpected death in epilepsy (SUDEP) accounts for up to 17 % of all these cases, which increases the rate of sudden death by 24-fold as compared to the general population. The underlying mechanisms are still not elucidated, but recent studies suggest the possibility that a common genetic channelopathy might contribute to both epilepsy and cardiac disease to increase the incidence of death via a lethal cardiac arrhythmia. We performed genetic testing in a large cohort of individuals with epilepsy and cardiac conduction disorders in order to identify genetic mutations that could play a role in the mechanism of sudden death. Putative pathogenic disease-causing mutations in genes encoding cardiac ion channel were detected in 24 % of unrelated individuals with epilepsy. Segregation analysis through genetic screening of the available family members and functional studies are crucial tasks to understand and to prove the possible pathogenicity of the variant, but in our cohort, only two families were available. Despite further research should be performed to clarify the mechanism of coexistence of both clinical conditions, genetic analysis, applied also in post-mortem setting, could be very useful to identify genetic factors that predispose epileptic patients to sudden death, helping to prevent sudden death in patients with epilepsy.

Item Type:Article
ID Code:10027
Uncontrolled Keywords:Sudden unexplained death in epilepsy, channelopathy, Long QT syndrome, Brugada syndrome, cardiac arrhythmias, epilepsy
Subjects:Area 06 - Scienze mediche > MED/26 Neurologia
Divisions:001 Università di Sassari > 01-a Nuovi Dipartimenti dal 2012 > Medicina Clinica e Sperimentale
Publisher:Springer Berlin Heidelberg
Deposited On:10 Sep 2014 08:57

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