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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...

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Autores principales: Chung, Chi-Ting, Lee, Ni-Chung, Fan, Sung-Pin, Hung, Miao-Zi, Lin, Yen-Heng, Chen, Chih-Hao, Jao, Tun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
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.
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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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