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DYNC1H1 variant associated with epilepsy: Expanding the phenotypic spectrum
DYNC1H1 variants are associated with peripheral neuronal dysfunction and brain morphology abnormalities resulting in neurodevelopmental delay. However, few studies have focused on the association between DYNC1H1 variants and epilepsy. Herein, we report a case of drug-resistant focal epilepsy associa...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9829698/ https://www.ncbi.nlm.nih.gov/pubmed/36636459 http://dx.doi.org/10.1016/j.ebr.2022.100580 |
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author | Chung, Chi-Ting Lee, Ni-Chung Fan, Sung-Pin Hung, Miao-Zi Lin, Yen-Heng Chen, Chih-Hao Jao, Tun |
author_facet | Chung, Chi-Ting Lee, Ni-Chung Fan, Sung-Pin Hung, Miao-Zi Lin, Yen-Heng Chen, Chih-Hao Jao, Tun |
author_sort | Chung, Chi-Ting |
collection | PubMed |
description | DYNC1H1 variants are associated with peripheral neuronal dysfunction and brain morphology abnormalities resulting in neurodevelopmental delay. However, few studies have focused on the association between DYNC1H1 variants and epilepsy. Herein, we report a case of drug-resistant focal epilepsy associated with a pathogenic variant of DYNC1H1. We further summarized the clinical, genetic, and neuroimaging characteristics of patients with DYNC1H1 variant–associated epilepsy from the relevant literature. This report expands the phenotypic spectrum of DYNC1H1-related disorder to include early-onset epilepsy, which is frequently associated with neurodevelopmental delay and intellectual disability, malformations of cortical development, and neuromuscular, ophthalmic, and orthopedic involvement. |
format | Online Article Text |
id | pubmed-9829698 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-98296982023-01-11 DYNC1H1 variant associated with epilepsy: Expanding the phenotypic spectrum Chung, Chi-Ting Lee, Ni-Chung Fan, Sung-Pin Hung, Miao-Zi Lin, Yen-Heng Chen, Chih-Hao Jao, Tun Epilepsy Behav Rep Case Report DYNC1H1 variants are associated with peripheral neuronal dysfunction and brain morphology abnormalities resulting in neurodevelopmental delay. However, few studies have focused on the association between DYNC1H1 variants and epilepsy. Herein, we report a case of drug-resistant focal epilepsy associated with a pathogenic variant of DYNC1H1. We further summarized the clinical, genetic, and neuroimaging characteristics of patients with DYNC1H1 variant–associated epilepsy from the relevant literature. This report expands the phenotypic spectrum of DYNC1H1-related disorder to include early-onset epilepsy, which is frequently associated with neurodevelopmental delay and intellectual disability, malformations of cortical development, and neuromuscular, ophthalmic, and orthopedic involvement. Elsevier 2022-12-28 /pmc/articles/PMC9829698/ /pubmed/36636459 http://dx.doi.org/10.1016/j.ebr.2022.100580 Text en © 2023 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Case Report Chung, Chi-Ting Lee, Ni-Chung Fan, Sung-Pin Hung, Miao-Zi Lin, Yen-Heng Chen, Chih-Hao Jao, Tun DYNC1H1 variant associated with epilepsy: Expanding the phenotypic spectrum |
title | DYNC1H1 variant associated with epilepsy: Expanding the phenotypic spectrum |
title_full | DYNC1H1 variant associated with epilepsy: Expanding the phenotypic spectrum |
title_fullStr | DYNC1H1 variant associated with epilepsy: Expanding the phenotypic spectrum |
title_full_unstemmed | DYNC1H1 variant associated with epilepsy: Expanding the phenotypic spectrum |
title_short | DYNC1H1 variant associated with epilepsy: Expanding the phenotypic spectrum |
title_sort | dync1h1 variant associated with epilepsy: expanding the phenotypic spectrum |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9829698/ https://www.ncbi.nlm.nih.gov/pubmed/36636459 http://dx.doi.org/10.1016/j.ebr.2022.100580 |
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