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Pattern and etiology of early childhood epilepsy: An Experience at a tertiary care University Center

OBJECTIVES: To investigate seizure characteristics, types, and define the etiology of epilepsy in children aged ≤2 years using the 2017 ILAE classification. METHODS: A retrospective chart review was conducted at King Khalid University Hospital, King Saud University Medical City, Riyadh, Kingdom of S...

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Autores principales: Kentab, Amal Y., Al Bulayhi, Shumukh, Hamad, Muddathir H., Al Wadei, Ali, Bashiri, Fahad A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Riyadh : Armed Forces Hospital 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9749570/
https://www.ncbi.nlm.nih.gov/pubmed/36252977
http://dx.doi.org/10.17712/nsj.2022.4.20220001
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author Kentab, Amal Y.
Al Bulayhi, Shumukh
Hamad, Muddathir H.
Al Wadei, Ali
Bashiri, Fahad A.
author_facet Kentab, Amal Y.
Al Bulayhi, Shumukh
Hamad, Muddathir H.
Al Wadei, Ali
Bashiri, Fahad A.
author_sort Kentab, Amal Y.
collection PubMed
description OBJECTIVES: To investigate seizure characteristics, types, and define the etiology of epilepsy in children aged ≤2 years using the 2017 ILAE classification. METHODS: A retrospective chart review was conducted at King Khalid University Hospital, King Saud University Medical City, Riyadh, Kingdom of Saudi Arabia for children below 2 years of age diagnosed with epilepsy, and on anti-seizure medications from January 2017 – December 2018. The collected data involved detailed information on the patients’ seizure, electroclinical, neuroimaging, laboratory evaluations, and underlying etiology. RESULTS: One- hundred and fifty patients were included in the study and classified according to etiology into: genetic (43, 28.7%), structural (41, 27.3%), metabolic (10, 6.7%), infectious (8, 5.3%), immune-mediated (1, 0.7%) and unknown (47, 31.3%) groups. The most common seizure types were generalized epilepsy, among which generalized tonic-clonic seizures occurred in 56 (37%) patients, followed by tonic seizures in 31 (21%), infantile spasm in 19 (13%), myoclonic seizures in 4 (2.7%), atonic seizures in 6 (4%), and focal seizures in 33 (22%) patients. Global developmental delay and abnormalities in both neurologic exam and neuroimaging were more common in the structural and genetic groups. Electroencephalography was abnormal in 82 (55%) patients, including the majority of the structural group (26, 63.4%). CONCLUSION: The etiology of epilepsy in this cohort remains undetermined (unknown) in a large proportion of cases, followed by genetic and structural causes. This result added to the published international data about epilepsy in the first 2-years of life.
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spelling pubmed-97495702023-01-04 Pattern and etiology of early childhood epilepsy: An Experience at a tertiary care University Center Kentab, Amal Y. Al Bulayhi, Shumukh Hamad, Muddathir H. Al Wadei, Ali Bashiri, Fahad A. Neurosciences (Riyadh) Original Article OBJECTIVES: To investigate seizure characteristics, types, and define the etiology of epilepsy in children aged ≤2 years using the 2017 ILAE classification. METHODS: A retrospective chart review was conducted at King Khalid University Hospital, King Saud University Medical City, Riyadh, Kingdom of Saudi Arabia for children below 2 years of age diagnosed with epilepsy, and on anti-seizure medications from January 2017 – December 2018. The collected data involved detailed information on the patients’ seizure, electroclinical, neuroimaging, laboratory evaluations, and underlying etiology. RESULTS: One- hundred and fifty patients were included in the study and classified according to etiology into: genetic (43, 28.7%), structural (41, 27.3%), metabolic (10, 6.7%), infectious (8, 5.3%), immune-mediated (1, 0.7%) and unknown (47, 31.3%) groups. The most common seizure types were generalized epilepsy, among which generalized tonic-clonic seizures occurred in 56 (37%) patients, followed by tonic seizures in 31 (21%), infantile spasm in 19 (13%), myoclonic seizures in 4 (2.7%), atonic seizures in 6 (4%), and focal seizures in 33 (22%) patients. Global developmental delay and abnormalities in both neurologic exam and neuroimaging were more common in the structural and genetic groups. Electroencephalography was abnormal in 82 (55%) patients, including the majority of the structural group (26, 63.4%). CONCLUSION: The etiology of epilepsy in this cohort remains undetermined (unknown) in a large proportion of cases, followed by genetic and structural causes. This result added to the published international data about epilepsy in the first 2-years of life. Riyadh : Armed Forces Hospital 2022-10 /pmc/articles/PMC9749570/ /pubmed/36252977 http://dx.doi.org/10.17712/nsj.2022.4.20220001 Text en Copyright: © Neurosciences https://creativecommons.org/licenses/by-nc/3.0/Neurosciences is an Open Access journal and articles published are distributed under the terms of the Creative Commons Attribution-NonCommercial License (CC BY-NC). Readers may copy, distribute, and display the work for non-commercial purposes with the proper citation of the original work.
spellingShingle Original Article
Kentab, Amal Y.
Al Bulayhi, Shumukh
Hamad, Muddathir H.
Al Wadei, Ali
Bashiri, Fahad A.
Pattern and etiology of early childhood epilepsy: An Experience at a tertiary care University Center
title Pattern and etiology of early childhood epilepsy: An Experience at a tertiary care University Center
title_full Pattern and etiology of early childhood epilepsy: An Experience at a tertiary care University Center
title_fullStr Pattern and etiology of early childhood epilepsy: An Experience at a tertiary care University Center
title_full_unstemmed Pattern and etiology of early childhood epilepsy: An Experience at a tertiary care University Center
title_short Pattern and etiology of early childhood epilepsy: An Experience at a tertiary care University Center
title_sort pattern and etiology of early childhood epilepsy: an experience at a tertiary care university center
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9749570/
https://www.ncbi.nlm.nih.gov/pubmed/36252977
http://dx.doi.org/10.17712/nsj.2022.4.20220001
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