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Seizure remission and improvement of neurological function in sialidosis with perampanel therapy
A 15-year-old boy experienced myoclonic seizures for 3 years. He initially had occasional myoclonus, gradually progressive ataxia, tremors, and psychomotor and speech regression developed. Eventually, he exhibited nearly continuous myoclonus. He received treatment of sodium valproate, levetiracetam,...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6030028/ https://www.ncbi.nlm.nih.gov/pubmed/29977792 http://dx.doi.org/10.1016/j.ebcr.2018.02.005 |
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author | Hu, Su-Ching Hung, Kun-Long Chen, Hui-Ju Lee, Wang-Tso |
author_facet | Hu, Su-Ching Hung, Kun-Long Chen, Hui-Ju Lee, Wang-Tso |
author_sort | Hu, Su-Ching |
collection | PubMed |
description | A 15-year-old boy experienced myoclonic seizures for 3 years. He initially had occasional myoclonus, gradually progressive ataxia, tremors, and psychomotor and speech regression developed. Eventually, he exhibited nearly continuous myoclonus. He received treatment of sodium valproate, levetiracetam, clobazam, and phenobarbital, without efficacy. A ketogenic diet also proved ineffective. Adjunctive therapy with 4 mg/day of perampanel was started and was gradually titrated to 10 mg/day. The remission of myoclonic seizures was achieved within one month. The patient's neurological and cognitive functions improved to a certain degree during the following 20 months. Sialidosis was confirmed by the mutations of NEU1 gene. |
format | Online Article Text |
id | pubmed-6030028 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-60300282018-07-05 Seizure remission and improvement of neurological function in sialidosis with perampanel therapy Hu, Su-Ching Hung, Kun-Long Chen, Hui-Ju Lee, Wang-Tso Epilepsy Behav Case Rep Article A 15-year-old boy experienced myoclonic seizures for 3 years. He initially had occasional myoclonus, gradually progressive ataxia, tremors, and psychomotor and speech regression developed. Eventually, he exhibited nearly continuous myoclonus. He received treatment of sodium valproate, levetiracetam, clobazam, and phenobarbital, without efficacy. A ketogenic diet also proved ineffective. Adjunctive therapy with 4 mg/day of perampanel was started and was gradually titrated to 10 mg/day. The remission of myoclonic seizures was achieved within one month. The patient's neurological and cognitive functions improved to a certain degree during the following 20 months. Sialidosis was confirmed by the mutations of NEU1 gene. Elsevier 2018-03-12 /pmc/articles/PMC6030028/ /pubmed/29977792 http://dx.doi.org/10.1016/j.ebcr.2018.02.005 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Hu, Su-Ching Hung, Kun-Long Chen, Hui-Ju Lee, Wang-Tso Seizure remission and improvement of neurological function in sialidosis with perampanel therapy |
title | Seizure remission and improvement of neurological function in sialidosis with perampanel therapy |
title_full | Seizure remission and improvement of neurological function in sialidosis with perampanel therapy |
title_fullStr | Seizure remission and improvement of neurological function in sialidosis with perampanel therapy |
title_full_unstemmed | Seizure remission and improvement of neurological function in sialidosis with perampanel therapy |
title_short | Seizure remission and improvement of neurological function in sialidosis with perampanel therapy |
title_sort | seizure remission and improvement of neurological function in sialidosis with perampanel therapy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6030028/ https://www.ncbi.nlm.nih.gov/pubmed/29977792 http://dx.doi.org/10.1016/j.ebcr.2018.02.005 |
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