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Clinical and Instrumental Characterization of Patients With Late-Onset Epilepsy
Epilepsy is classically considered a childhood disease. However, it represents the third most frequent neurological condition in the elderly, following stroke, and dementia. With the progressive aging of the general population, the number of patients with Late-Onset Epilepsy (LOE) is constantly grow...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8963711/ https://www.ncbi.nlm.nih.gov/pubmed/35359649 http://dx.doi.org/10.3389/fneur.2022.851897 |
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author | DiFrancesco, Jacopo C. Labate, Angelo Romoli, Michele Chipi, Elena Salvadori, Nicola Galimberti, Carlo Andrea Perani, Daniela Ferrarese, Carlo Costa, Cinzia |
author_facet | DiFrancesco, Jacopo C. Labate, Angelo Romoli, Michele Chipi, Elena Salvadori, Nicola Galimberti, Carlo Andrea Perani, Daniela Ferrarese, Carlo Costa, Cinzia |
author_sort | DiFrancesco, Jacopo C. |
collection | PubMed |
description | Epilepsy is classically considered a childhood disease. However, it represents the third most frequent neurological condition in the elderly, following stroke, and dementia. With the progressive aging of the general population, the number of patients with Late-Onset Epilepsy (LOE) is constantly growing, with important economic and social consequences, in particular for the more developed countries where the percentage of elderly people is higher. The most common causes of LOE are structural, mainly secondary to cerebrovascular or infectious diseases, brain tumors, trauma, and metabolic or toxic conditions. Moreover, there is a growing body of evidence linking LOE with neurodegenerative diseases, particularly Alzheimer's disease (AD). However, despite a thorough characterization, the causes of LOE remain unknown in a considerable portion of patients, thus termed as Late-Onset Epilepsy of Unknown origin (LOEU). In order to identify the possible causes of the disease, with an important impact in terms of treatment and prognosis, LOE patients should always undergo an exhaustive phenotypic characterization. In this work, we provide a detailed review of the main clinical and instrumental techniques for the adequate characterization of LOE patients in the clinical practice. This work aims to provide an easy and effective tool that supports routine activity of the clinicians facing LOE. |
format | Online Article Text |
id | pubmed-8963711 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-89637112022-03-30 Clinical and Instrumental Characterization of Patients With Late-Onset Epilepsy DiFrancesco, Jacopo C. Labate, Angelo Romoli, Michele Chipi, Elena Salvadori, Nicola Galimberti, Carlo Andrea Perani, Daniela Ferrarese, Carlo Costa, Cinzia Front Neurol Neurology Epilepsy is classically considered a childhood disease. However, it represents the third most frequent neurological condition in the elderly, following stroke, and dementia. With the progressive aging of the general population, the number of patients with Late-Onset Epilepsy (LOE) is constantly growing, with important economic and social consequences, in particular for the more developed countries where the percentage of elderly people is higher. The most common causes of LOE are structural, mainly secondary to cerebrovascular or infectious diseases, brain tumors, trauma, and metabolic or toxic conditions. Moreover, there is a growing body of evidence linking LOE with neurodegenerative diseases, particularly Alzheimer's disease (AD). However, despite a thorough characterization, the causes of LOE remain unknown in a considerable portion of patients, thus termed as Late-Onset Epilepsy of Unknown origin (LOEU). In order to identify the possible causes of the disease, with an important impact in terms of treatment and prognosis, LOE patients should always undergo an exhaustive phenotypic characterization. In this work, we provide a detailed review of the main clinical and instrumental techniques for the adequate characterization of LOE patients in the clinical practice. This work aims to provide an easy and effective tool that supports routine activity of the clinicians facing LOE. Frontiers Media S.A. 2022-02-25 /pmc/articles/PMC8963711/ /pubmed/35359649 http://dx.doi.org/10.3389/fneur.2022.851897 Text en Copyright © 2022 DiFrancesco, Labate, Romoli, Chipi, Salvadori, Galimberti, Perani, Ferrarese and Costa. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neurology DiFrancesco, Jacopo C. Labate, Angelo Romoli, Michele Chipi, Elena Salvadori, Nicola Galimberti, Carlo Andrea Perani, Daniela Ferrarese, Carlo Costa, Cinzia Clinical and Instrumental Characterization of Patients With Late-Onset Epilepsy |
title | Clinical and Instrumental Characterization of Patients With Late-Onset Epilepsy |
title_full | Clinical and Instrumental Characterization of Patients With Late-Onset Epilepsy |
title_fullStr | Clinical and Instrumental Characterization of Patients With Late-Onset Epilepsy |
title_full_unstemmed | Clinical and Instrumental Characterization of Patients With Late-Onset Epilepsy |
title_short | Clinical and Instrumental Characterization of Patients With Late-Onset Epilepsy |
title_sort | clinical and instrumental characterization of patients with late-onset epilepsy |
topic | Neurology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8963711/ https://www.ncbi.nlm.nih.gov/pubmed/35359649 http://dx.doi.org/10.3389/fneur.2022.851897 |
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