Idiopathic and symptomatic forms of genetic epilepsy
According to the new classification of the epilepsies proposed in 2017 by The International League Against Epilepsy, idiopathic epilepsies are recommended to refer to genetic epilepsy, suggesting to consider the term “idiopathic” as outdated. In connection with this, a tendency arose to refer fo...
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Format: | Article |
Language: | Russian |
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IRBIS LLC
2022-04-01
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Series: | Эпилепсия и пароксизмальные состояния |
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Online Access: | https://www.epilepsia.su/jour/article/view/778 |
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author | A. G. Malov |
author_facet | A. G. Malov |
author_sort | A. G. Malov |
collection | DOAJ |
description | According to the new classification of the epilepsies proposed in 2017 by The International League Against Epilepsy, idiopathic epilepsies are recommended to refer to genetic epilepsy, suggesting to consider the term “idiopathic” as outdated. In connection with this, a tendency arose to refer forms of epilepsy previously called “idiopathic” as genetic epilepsy. However, idiopathic epilepsy constitutes just a part among genetic epilepsies. The other groups resulting from this etiology are monogenic epilepsies (e.g., Dravet syndrome) as well as symptomatic epilepsies due to other genetically determined syndromes (e.g., biotinidase deficiency or neuronal ceroid lipofuscinosis). The distinction between the three groups comprising genetic epilepsy is important not only due to difference in related etiology and course, but also because specific treatment in some monogenic forms might be possible. Here, the major criteria for distinguishing between such epilepsy groups are presented. |
first_indexed | 2024-04-10T02:47:19Z |
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id | doaj.art-f7f8d3cbee524589b6b68751f1822e19 |
institution | Directory Open Access Journal |
issn | 2077-8333 2311-4088 |
language | Russian |
last_indexed | 2025-03-14T11:13:34Z |
publishDate | 2022-04-01 |
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series | Эпилепсия и пароксизмальные состояния |
spelling | doaj.art-f7f8d3cbee524589b6b68751f1822e192025-03-02T10:17:07ZrusIRBIS LLCЭпилепсия и пароксизмальные состояния2077-83332311-40882022-04-01141919510.17749/2077-8333/epi.par.con.2022.107575Idiopathic and symptomatic forms of genetic epilepsyA. G. Malov0Vagner Perm State Medical UniversityAccording to the new classification of the epilepsies proposed in 2017 by The International League Against Epilepsy, idiopathic epilepsies are recommended to refer to genetic epilepsy, suggesting to consider the term “idiopathic” as outdated. In connection with this, a tendency arose to refer forms of epilepsy previously called “idiopathic” as genetic epilepsy. However, idiopathic epilepsy constitutes just a part among genetic epilepsies. The other groups resulting from this etiology are monogenic epilepsies (e.g., Dravet syndrome) as well as symptomatic epilepsies due to other genetically determined syndromes (e.g., biotinidase deficiency or neuronal ceroid lipofuscinosis). The distinction between the three groups comprising genetic epilepsy is important not only due to difference in related etiology and course, but also because specific treatment in some monogenic forms might be possible. Here, the major criteria for distinguishing between such epilepsy groups are presented.https://www.epilepsia.su/jour/article/view/778genetic epilepsyidiopathic epilepsymonogenic epilepsygenetically determined syndrome |
spellingShingle | A. G. Malov Idiopathic and symptomatic forms of genetic epilepsy Эпилепсия и пароксизмальные состояния genetic epilepsy idiopathic epilepsy monogenic epilepsy genetically determined syndrome |
title | Idiopathic and symptomatic forms of genetic epilepsy |
title_full | Idiopathic and symptomatic forms of genetic epilepsy |
title_fullStr | Idiopathic and symptomatic forms of genetic epilepsy |
title_full_unstemmed | Idiopathic and symptomatic forms of genetic epilepsy |
title_short | Idiopathic and symptomatic forms of genetic epilepsy |
title_sort | idiopathic and symptomatic forms of genetic epilepsy |
topic | genetic epilepsy idiopathic epilepsy monogenic epilepsy genetically determined syndrome |
url | https://www.epilepsia.su/jour/article/view/778 |
work_keys_str_mv | AT agmalov idiopathicandsymptomaticformsofgeneticepilepsy |