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Case report: Young-onset large vessel ischemic stroke due to hyperhomocysteinemia associated with the C677T polymorphism on 5,10-methylenetetrahydrofolate reductase and multi-vitamin deficiency
Hyperhomocysteinemia is an important risk factor for cerebral infarction. Herein, we report on a 30-year-old man previously diagnosed with epilepsy who presented with right hemiplegia and total aphasia. Magnetic resonance imaging showed a fronto-temporal ischemic lesion due to occlusion of the left...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10233819/ https://www.ncbi.nlm.nih.gov/pubmed/37273715 http://dx.doi.org/10.3389/fneur.2023.1183306 |
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author | Fukae, Jiro Eguchi, Hiroto Wada, Yoichi Fuse, Atsuhito Chishima, Rika Nakatani, Mitsuyoshi Nakajima, Asuka Hattori, Nobutaka Shimo, Yasushi |
author_facet | Fukae, Jiro Eguchi, Hiroto Wada, Yoichi Fuse, Atsuhito Chishima, Rika Nakatani, Mitsuyoshi Nakajima, Asuka Hattori, Nobutaka Shimo, Yasushi |
author_sort | Fukae, Jiro |
collection | PubMed |
description | Hyperhomocysteinemia is an important risk factor for cerebral infarction. Herein, we report on a 30-year-old man previously diagnosed with epilepsy who presented with right hemiplegia and total aphasia. Magnetic resonance imaging showed a fronto-temporal ischemic lesion due to occlusion of the left middle cerebral artery. Clinical testing and imaging demonstrated that he had hyperhomocysteinemia induced by multiple factors including the C677T polymorphism on 5.10-methylenetetrahydrofolate reductase (MTHFR), and multiple vitamin deficiencies. The C677T polymorphism on MTHFR is closely related to hyperhomocysteinemia and folate deficiency in epileptic patients who are taking multiple anti-convulsants. Given hyperhomocysteinemia can independently cause stroke at a young age, physicians should periodically examine plasma homocysteine and serum folic acid levels in epileptic patients who are on long-term regimens of multiple anti-epileptic drugs. |
format | Online Article Text |
id | pubmed-10233819 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102338192023-06-02 Case report: Young-onset large vessel ischemic stroke due to hyperhomocysteinemia associated with the C677T polymorphism on 5,10-methylenetetrahydrofolate reductase and multi-vitamin deficiency Fukae, Jiro Eguchi, Hiroto Wada, Yoichi Fuse, Atsuhito Chishima, Rika Nakatani, Mitsuyoshi Nakajima, Asuka Hattori, Nobutaka Shimo, Yasushi Front Neurol Neurology Hyperhomocysteinemia is an important risk factor for cerebral infarction. Herein, we report on a 30-year-old man previously diagnosed with epilepsy who presented with right hemiplegia and total aphasia. Magnetic resonance imaging showed a fronto-temporal ischemic lesion due to occlusion of the left middle cerebral artery. Clinical testing and imaging demonstrated that he had hyperhomocysteinemia induced by multiple factors including the C677T polymorphism on 5.10-methylenetetrahydrofolate reductase (MTHFR), and multiple vitamin deficiencies. The C677T polymorphism on MTHFR is closely related to hyperhomocysteinemia and folate deficiency in epileptic patients who are taking multiple anti-convulsants. Given hyperhomocysteinemia can independently cause stroke at a young age, physicians should periodically examine plasma homocysteine and serum folic acid levels in epileptic patients who are on long-term regimens of multiple anti-epileptic drugs. Frontiers Media S.A. 2023-05-18 /pmc/articles/PMC10233819/ /pubmed/37273715 http://dx.doi.org/10.3389/fneur.2023.1183306 Text en Copyright © 2023 Fukae, Eguchi, Wada, Fuse, Chishima, Nakatani, Nakajima, Hattori and Shimo. 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 Fukae, Jiro Eguchi, Hiroto Wada, Yoichi Fuse, Atsuhito Chishima, Rika Nakatani, Mitsuyoshi Nakajima, Asuka Hattori, Nobutaka Shimo, Yasushi Case report: Young-onset large vessel ischemic stroke due to hyperhomocysteinemia associated with the C677T polymorphism on 5,10-methylenetetrahydrofolate reductase and multi-vitamin deficiency |
title | Case report: Young-onset large vessel ischemic stroke due to hyperhomocysteinemia associated with the C677T polymorphism on 5,10-methylenetetrahydrofolate reductase and multi-vitamin deficiency |
title_full | Case report: Young-onset large vessel ischemic stroke due to hyperhomocysteinemia associated with the C677T polymorphism on 5,10-methylenetetrahydrofolate reductase and multi-vitamin deficiency |
title_fullStr | Case report: Young-onset large vessel ischemic stroke due to hyperhomocysteinemia associated with the C677T polymorphism on 5,10-methylenetetrahydrofolate reductase and multi-vitamin deficiency |
title_full_unstemmed | Case report: Young-onset large vessel ischemic stroke due to hyperhomocysteinemia associated with the C677T polymorphism on 5,10-methylenetetrahydrofolate reductase and multi-vitamin deficiency |
title_short | Case report: Young-onset large vessel ischemic stroke due to hyperhomocysteinemia associated with the C677T polymorphism on 5,10-methylenetetrahydrofolate reductase and multi-vitamin deficiency |
title_sort | case report: young-onset large vessel ischemic stroke due to hyperhomocysteinemia associated with the c677t polymorphism on 5,10-methylenetetrahydrofolate reductase and multi-vitamin deficiency |
topic | Neurology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10233819/ https://www.ncbi.nlm.nih.gov/pubmed/37273715 http://dx.doi.org/10.3389/fneur.2023.1183306 |
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